홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 612814
노트
인쇄 미리보기

반응식

HRID 612814 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 165294Benzyltriethylammonium bromide촉매HCID 14798
Sodium Hydroxide
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-65b1e7d3fc794e8282339830fb07881d
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06005102

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트