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Water → 17-Bromoheptadec-6-en-1-ol

HRID 1756487
ノート
印刷プレビュー

反応式

HRID 1756487 の反応式
[Br-].[OH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[Br:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45]O.O>ClCCl.O1CCCC1>[Br:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH:45]=[CH:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][OH:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 7416311-Bromo-1-undecanolHCID 2784664Phosphonium, (6-hydroxyhexyl)triphenyl-, bromideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 5368882717-Bromoheptadec-6-en-1-ol収率 45.8%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane
溶媒
HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of (6-hydroxyhexyl)triphenylphosphonium bromide (5.0 g) in dichloromethane (20 ml) was added dropwise to a mixture of potassium tertiary-butoxide (2.8 g) in tetrahydrofuran (100 ml) at 5°. After ten minutes, 11-bromoundecanol (2.8 g) in tetrahydrofuran (20 ml) was added and the reaction stirred at 5° until TLC indicated completion of the reaction. Water (20 ml) was added and the mixture then concentrated in vacuo. Water (20 ml) was added to the residue and the aqueous phase extracted with ether (2×50 ml). The combined organic extracts were dried (MgSO4) and concentrated in vacuo to give a brown oil. This was subjected to column chromatography to yield 17-bromoheptadec-6-en-1-ol (1.7 g, 45%).

後処理

  1. waitAfter ten minutes
  2. customcompletion of the reaction
  3. concentrationthe mixture then concentrated in vacuo
  4. additionWater (20 ml) was added to the residue
  5. extractionthe aqueous phase extracted with ether (2×50 ml)
  6. dry with materialThe combined organic extracts were dried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customto give a brown oil

出典と根拠

ORDレコード
ord-3d8c8c6c97a24d6d99f70e7075a22ca2
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05441731

反応ノート

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