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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Propargyl alcohol → Nonadec-2-yn-1-ol

HRID 248149
노트
인쇄 미리보기

반응식

HRID 248149 반응식
[CH2:1]([OH:4])[C:2]#[CH:3].[Li].[CH2:6](Br)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]>O1CCCC1.N>[CH2:1]([OH:4])[C:2]#[C:3][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7859Propargyl alcoholHCID 82131-BromohexadecaneHCID 3028194Lithium

생성물 1

HCID 10967930Nonadec-2-yn-1-ol

시약·촉매·용매 2

HCID 222Ammonia용매HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 56.1 g of propargyl alcohol in 100 ml of tetrahydrofuran and 15.6 g of lithium in 1 liter of ammonia containing a trace of ferric chloride is stirred for 1 hour. A 76.4 ml portion of hexadecyl bromide is added and the mixture refluxed for 8 hours then evaporated. The residue is dissolved in ether and washed with 10% hydrochloric acid, dried and purified by flash chromatography, to give 47.4 g of the desired compound as white platelets, mp. 60° C.

후처리

  1. temperaturethe mixture refluxed for 8 hours
  2. customthen evaporated
  3. dissolutionThe residue is dissolved in ether
  4. washwashed with 10% hydrochloric acid
  5. customdried
  6. custompurified by flash chromatography

출처 및 근거

ORD 기록
ord-03ad03efdbea4d5a919894b5736fd45f
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05208223

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