反应 #4162685
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ec278794e22b49e6a0921689b46b256c暂无可渲染的结构数据
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乳酸苄酯(CAS 2051-96-9)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ec278794e22b49e6a0921689b46b256c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d20cb56cf2534038bab7ed7a20c2dcc9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f6838e61a1b741879e2ef468db155d1b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-18d9f8f0df9d41318ab43f3a1d450cde反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ec278794e22b49e6a0921689b46b256c反应条件: temp:-15.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Construction of Benzyl-L-lactic Acid. L-Lactic acid (9 g, 100 mmol) is added to N,N'-diisopropylbenzylisourea (23.3 g, 100 mmol) with stirring. The mixture becomes very viscous within 10 min and is stirred intermittently for 1 h. The volume is then increased to 200 mL with THF, and the mixture stirred for 48 h at room temperature. After cooling the mixture to -15° C., the diisopropylurea is removed by filtration and the THF is evaporated under reduced pressure. The resulting thick oil is pumped under high vacuum for 24 h to give benzyl lactate (17.4 g, 95%) which may be used without further purification. is stirred intermittently for 1 h the mixture stirred for 48 h at room temperature the diisopropylurea is removed by filtration the THF is evaporated under reduced pressure The resulting thick oil is pumped under high vacuum for 24 h
来源 ID: ord-9f8135fc2ea3458ea13011035828fec5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d20cb56cf2534038bab7ed7a20c2dcc9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f6838e61a1b741879e2ef468db155d1b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-18d9f8f0df9d41318ab43f3a1d450cde反应条件: temp:-15.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Construction of Benzyl-L-lactic Acid. L-Lactic acid (9 g, 100 mmol) is added to N,N'-diisopropylbenzylisourea (23.3 g, 100 mmol) with stirring. The mixture becomes very viscous within 10 min and is stirred intermittently for 1 h. The volume is then increased to 200 mL with THF, and the mixture stirred for 48 h at room temperature. After cooling the mixture to -15° C., the diisopropylurea is removed by filtration and the THF is evaporated under reduced pressure. The resulting thick oil is pumped under high vacuum for 24 h to give benzyl lactate (17.4 g, 95%) which may be used without further purification. is stirred intermittently for 1 h the mixture stirred for 48 h at room temperature the diisopropylurea is removed by filtration the THF is evaporated under reduced pressure The resulting thick oil is pumped under high vacuum for 24 h
来源 ID: ord-9f8135fc2ea3458ea13011035828fec5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Reaction Scheme A above begins with the triflate of a carboxyl-protected D-αhydroxycarboxylic acid derivative, e.g., lactic acid benzyl ester. By reacting this triflate with α-ethyl-γ-anilido-L-glutamate (prepared, for example, by reacting an amino-protected L-glutamic acid, such as Nα -Cbo-L-glutamic acid, with diethyl sulfate in triethylamine and dichloromethane at room temperature for about three days to give Nα -Cbo-α-ethyl-L-glutamate, forming the dicyclohexylamine salt of the thus-obtained glutamate by reaction with dicyclohexylamine in ethyl acetate at room temperature overnight, acidifying a suspension of the dicyclohexylamine salt and then reacting the isolated free acid with dicyclohexylcarbodiimide and aniline in dichloromethane, first in a dry ice/ice/acetone bath for one hour, and then at room temperature overnight), Nα -[1(L)-carbethoxy-3-carboxanilidopropyl]-L alanine benzyl ester is obtained. Reaction Scheme A
来源 ID: ord-e9b05a6d4a554cc5bf3c38bb7c250d78反应条件: temp:-15.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Construction of Benzyl-L-lactic Acid. L-Lactic acid (9 g, 100 mmol) is added to N,N'-diisopropylbenzylisourea (23.3 g, 100 mmol) with stirring. The mixture becomes very viscous within 10 min and is stirred intermittently for 1 h. The volume is then increased to 200 mL with THF, and the mixture stirred for 48 h at room temperature. After cooling the mixture to -15° C., the diisopropylurea is removed by filtration and the THF is evaporated under reduced pressure. The resulting thick oil is pumped under high vacuum for 24 h to give benzyl lactate (17.4 g, 95%) which may be used without further purification. is stirred intermittently for 1 h the mixture stirred for 48 h at room temperature the diisopropylurea is removed by filtration the THF is evaporated under reduced pressure The resulting thick oil is pumped under high vacuum for 24 h
来源 ID: ord-ac871ceb01844d57beddf303b82b968dPubChem References
以下资料来自该化合物的公开数据库参考记录。
