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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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4-(5-Cyclopropylamino-8,8-dimethyl-5,6,7,8-tetrahydro-naphthalene-2-ylethynyl)-benzoic acid ethyl ester → 6-Bromo-8-vinyl-2,2,4,4-tetramethyl-chroman

HRID 381045
ノート
印刷プレビュー

反応式

HRID 381045 の反応式
[CH2:1](OC(=O)C1C=CC(C#CC2C=CC3C(NC4CC4)CCC(C)(C)C=3C=2)=CC=1)C.[Br:30][C:31]1[CH:32]=[C:33]2[C:38](=[C:39]([CH:41]=O)[CH:40]=1)[O:37][C:36]([CH3:44])([CH3:43])[CH2:35][C:34]2([CH3:46])[CH3:45]>CCCCCC>[Br:30][C:31]1[CH:32]=[C:33]2[C:38](=[C:39]([CH:41]=[CH2:1])[CH:40]=1)[O:37][C:36]([CH3:44])([CH3:43])[CH2:35][C:34]2([CH3:46])[CH3:45]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 129717084-(5-Cyclopropylamino-8,8-dimethyl-5,6,7,8-tetrahydro-naphthalene-2-ylethynyl)-benzoic acid ethyl ester2 回HCID 225689466-Bromo-2,2,4,4-tetramethyl chroman-8-carbaldehyde2 回

生成物 1

HCID 225689226-Bromo-8-vinyl-2,2,4,4-tetramethyl-chroman収率 72%

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

A solution of methylidene triphenyl phosphorane [generated from methyl triphenylphosphonium bromide (7 g, 20 mmol) and (11.8 mL, 19 mmol) of a 1 .6M solution of n-butyl lithium in hexanes] was added 6-bromo-2,2,4,4-tetramethyl chroman-8-carbaldehyde (Intermediate 30, 0.52 g, 1.75 mmol). After 1 h the reaction mixture was diluted with hexane, washed with brine (×1), dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to a clear oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using 2% ethyl acetate in hexane as the eluent to afford the title compound as a clear oil (0.37 g, 72%).

後処理

  1. washwashed with brine (×1)
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. customevaporated in vacuo to a clear oil which

出典と根拠

ORDレコード
ord-569bd1803482404f9f8d5e5557063fa1
出典データセット
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06303785B1

反応ノート

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