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【结 构 式】

【分子编号】59142

【品名】methyl 2-bromo-4-oxopentanoate

【CA登记号】

【 分 子 式 】C6H9BrO3

【 分 子 量 】209.03966

【元素组成】C 34.47% H 4.34% Br 38.22% O 22.96%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(II)

Methyl acetylacrylate (III) was obtained by bromination of methyl levulinate (I) followed by dehydrohalogenation of the resultant bromide (II). Isonitrosation of ketone (III) by means of ethyl nitrite in ethereal HCl produced the alpha-keto oxime (IV). Reduction of oxime (IV) and simultaneous ester hydrolysis by means of Sn/SnCl2 in concentrated HCl led to the target 5-aminolevulinic acid.

1 Corwin, A.H.; Wynn, R.W.; The hydrogenation of oxaloacetone. A new synthesis of beta-thiolimidazolylpropionic acid. J Org Chem 1950, 15, 203.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 50960 Methyl levulinate C6H10O3 详情 详情
(II) 59142 methyl 2-bromo-4-oxopentanoate C6H9BrO3 详情 详情
(III) 59143 Methyl trans-beta-acetylacrylate; Methyl trans-4-oxo-2-pentenoate C6H8O3 详情 详情
(IV) 59144 methyl (E)-5-(hydroxyimino)-4-oxo-2-pentenoate C6H7NO4 详情 详情
Extended Information