tert-Butyl 2-bromo-2-methylpropionate → 2-(2-t-Butoxycarbonylprop-2-yloxyimino)-2-(thien-2-yl)acetic acid

HRID 839454

反応式

HRID 839454 の反応式
[OH:1][N:2]=[C:3]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[C:4]([OH:6])=[O:5].Br[C:13]([CH3:22])([CH3:21])[C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15].C([NH2+]CCC1C=CC=CC=1)C1C=CC=CC=1>C(O)C>[C:17]([O:16][C:14]([C:13]([O:1][N:2]=[C:3]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[C:4]([OH:6])=[O:5])([CH3:22])[CH3:21])=[O:15])([CH3:20])([CH3:19])[CH3:18]

参加物

5

反応物 3

HCID 90290tert-Butyl 2-bromo-2-methylpropionateHCID 1549262Benethamine(1+)HCID 736296442-Hydroxyimino(thien-2-yl)acetic acid

生成物 1

HCID 543000392-(2-t-Butoxycarbonylprop-2-yloxyimino)-2-(thien-2-yl)acetic acid収率 78%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

The title compound was prepared from 2-hydroxyimino-2-(thien-2-yl)acetic acid (syn isomer) and t-butyl 2-bromo-2-methylpropionate, in a similar manner to that described for Preparation 5, in 78% yield as a colourless oil, and was characterised as the N-benzyl-2-phenylethylammonium salt, m.p. 201.3°-201.9° (from ethanol).

後処理

  1. customdescribed for Preparation 5, in 78% yield as a colourless oil

出典と根拠

ORDレコード
ord-a60d37966a5a44a4a03264080324f276
出典データセット
uspto-grants-1978_06
特許番号
US04095021

関連ノート

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