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4-Hydroxybenzyl Alcohol → [4-(2-Piperidin-1-ylethoxy)phenyl]methanol

HRID 612814
ノート
印刷プレビュー

反応式

HRID 612814 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][OH:7])=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.Cl.Cl[CH2:19][CH2:20][N:21]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1>[OH-].[Na+].[Br-].C([N+](CC)(CC)CC)C1C=CC=CC=1>[N:21]1([CH2:20][CH2:19][O:1][C:2]2[CH:9]=[CH:8][C:5]([CH2:6][OH:7])=[CH:4][CH:3]=2)[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 1254-Hydroxybenzyl AlcoholHCID 1140TolueneHCID 74826Piperidine, 1-(2-chloroethyl)-, hydrochloride

生成物 1

HCID 9816107[4-(2-Piperidin-1-ylethoxy)phenyl]methanol収率 75%

試薬・触媒・溶媒 2

HCID 165294Benzyltriethylammonium bromide触媒HCID 14798
Sodium Hydroxide
溶媒

実験手順

4-hydroxybenzyl alcohol (6.2 g, 0.0.05 mol) was dissolved in aqueus sodium hydroxide (SN, 30 mL). Toluene (30 mL) was added followed by 1-(2-chloroethyl) piperidine hydrochloride (9.29 g, 0.05 mol) and benzyltriethylammonium bromide (0.3 g). The reaction mixture was heated with vigorous stirring for 1.5 h. The layers were separated, the aqueous layer was extracted with toluene (2×15 mL). Combined organic extracts and organic layer was washed with water (50 mL), brine (50 mL), dried over sodium sulfate, and concentrated on a rotary evaporator to give 8.725 g (75%) of alcohol (3a) as a yellowish brown oil.

後処理

  1. temperatureThe reaction mixture was heated
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with toluene (2×15 mL)
  4. washCombined organic extracts and organic layer was washed with water (50 mL), brine (50 mL)
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated on a rotary evaporator

出典と根拠

ORDレコード
ord-65b1e7d3fc794e8282339830fb07881d
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06005102

反応ノート

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