反应 #4086775
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-d529e475fceb4f26ba33c6c7349821a2暂无可渲染的结构数据
CCOC(=O)C(C)(C)N产品信息
2-氨基-2-甲基丙酸乙酯(CAS 1113-49-1)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-d529e475fceb4f26ba33c6c7349821a2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3f15926cb8074f5aa0bf0bce50ca80c2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ba5d4f6a8fe642d58007b0a75519c712反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-08406aeba510443d8e366c4f29941312反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7dc55ded984744aaaff52a8405301259反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9dae891804ed41b787d5a2963602efc7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-aminoisobutyric acid (3.3 g, 32 mmol) in absolute ethanol (100 mL) was cooled to −78° C. and HCl(g) bubbled in for 10 minutes. The flask was sealed with a septum and stirred at ambient temperature. After 14 hours the mixture was concentrated in vacuo to afford 5.3 g (99% yield) of ethyl 2-aminoisobutyrate as a white solid; NMR (CDCl3) 8.9 (br s, 3), 4.1 (q, 2), 1.7 (s, 6), 1.3 (t, 3) ppm. HCl(g) bubbled in for 10 minutes The flask was sealed with a septum After 14 hours the mixture was concentrated in vacuo
来源 ID: ord-2ecfcf1539fc4aed80c138a53997c200反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-2-methyl-propionic acid (1.0 g, 9.69 mmol) was dissolved in ethanol (15 ml) and cooled to 0° C. Thionyl chloride (1.7 g, 14.53 mmol, 1.5 eq) was added to the reaction mixture, which was then heated to reflux overnight. The solvent was evaporated and the residue was partitioned between water and ethyl acetate. The organic layer was concentrated and dried to give 2-amino-2-methyl-propionic acid ethyl ester (0.8 g, 63%). The crude compound was used in the next stage without purification. was then heated to reflux overnight The solvent was evaporated the residue was partitioned between water and ethyl acetate The organic layer was concentrated dried
来源 ID: ord-b9501f6ba7be4d5b99e63345d16d1dfc反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-2-methyl-propionic acid (1.0 g, 9.69 mmol) was dissolved in ethanol (15 ml) and cooled to 0° C. Thionyl chloride (1.7 g, 14.53 mmol, 1.5 eq) was added to the reaction mixture, which was then heated to reflux overnight. The solvent was evaporated and the residue was partitioned between water and ethyl acetate. The organic layer was concentrated and dried to give 2-amino-2-methyl-propionic acid ethyl ester (0.8 g, 63%). The crude compound was used in the next stage without purification. was then heated to reflux overnight The solvent was evaporated the residue was partitioned between water and ethyl acetate The organic layer was concentrated dried
来源 ID: ord-b9501f6ba7be4d5b99e63345d16d1dfc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d529e475fceb4f26ba33c6c7349821a2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3f15926cb8074f5aa0bf0bce50ca80c2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ba5d4f6a8fe642d58007b0a75519c712PubChem References
以下资料来自该化合物的公开数据库参考记录。
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