反应 #4124278
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-d930297e30194640a1ba1351cd9dc4c6暂无可渲染的结构数据
CCC(C(=O)OC(C)(C)C)Br产品信息
2-溴丁酸叔丁酯(CAS 24457-21-4)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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合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d930297e30194640a1ba1351cd9dc4c6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-19f9e5a33814420daf8f4ea674b2c42b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0bb480b2dc7f43149fef474dac5d6345反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fbb7ee4ab541498da8f571eb585416e5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8d11bb64d76a4a718cf541b1e24643fc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0c706c462938411199157ad31ccfa705反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Tert-butyl 2-(4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)-phenoxy)butanoate is prepared from 3-(4-hydroxyphenyl)-1-(5-(4-(trifluoromethyl)-phenyl)thien-2-yl)propan-1-one and tert-butyl 2-bromobutanoate according to general procedure D.
来源 ID: ord-88160b5a21ad4c47ad43a4313a0f5131反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Tert-butyl 2-(2-bromo-4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)phenoxy)-butanoate is prepared from 3-(3-bromo-4-hydroxyphenyl)-1-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propan-1-one and tert-butyl 2-bromobutanoate according to general procedure D.
来源 ID: ord-d320e170e060487e923d91b14512702a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Tert-butyl 2-(2-fluoro-4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)phenoxy)-butanoate is prepared from 3-(3-fluoro-4-hydroxyphenyl)-1-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propan-1-one and tert-butyl 2-bromobutanoate according to general procedure D.
来源 ID: ord-327c7d9a7166481da7ab3618a2d42192反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Tert-butyl 2-(2,3-dichloro-4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)phenoxy)-butanoate is prepared from 3-(2,3-dichloro-4-hydroxyphenyl)-1-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propan-1-one and tert-butyl 2-bromobutanoate according to general procedure D.
来源 ID: ord-884b4be70f9d47fc82791fe60d0e61c5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Examples 10 and 11 provide a detailed description for the preparation of (5S)-5-(N,N-dibenzylamino)-2-ethyl-4-oxo-hexanoic acid-tert-butyl ester from tert-butyl-2-bromobutyrate and α-(N,N-dibenzylamino)ethyl methyl ketone. This compound is reduced to the corresponding amino alcohol as described in detail above. Examples 10 and 11 provide a detailed description
来源 ID: ord-213729b141184971b1ce39abacdb58dc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Examples 10 and 11 provide a detailed description for the preparation of (5S)-5-(N,N-dibenzylamino)-2-ethyl-4-oxo-hexanoic acid-tert-butyl ester from tert-butyl-2-bromobutyrate and α-(N,N-dibenzylamino)ethyl methyl ketone. This compound is reduced to the corresponding amino alcohol as described in detail above. Examples 10 and 11 provide a detailed description
来源 ID: ord-213729b141184971b1ce39abacdb58dcPubChem References
以下资料来自该化合物的公开数据库参考记录。
