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

Nicotinic Acid → Nicotinoyl chloride

HRID 5011
노트
인쇄 미리보기

반응식

HRID 5011 반응식
[C:1]([OH:9])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.S(Cl)([Cl:12])=O.C(C1C=CC(OCCCCO)=CC=1)(C)(C)C>ClCCl>[C:1]([Cl:12])(=[O:9])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 938Nicotinic AcidHCID 24386Thionyl ChlorideHCID 133137374-(4-Tert-butylphenoxy)butan-1-OL

생성물 1

HCID 82604Nicotinoyl chloride

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Nicotinoyl chloride was prepared by treating 100 g (0.81 mole) of nicotinic acid with 280 ml of thionyl chloride at reflux for two hours. The excess thionyl chloride was removed in vacuo and the crystalline acid chloride hydrochloride was suspended in 500 ml of dichloromethane. To the stirred mixture was added 66 g (0.30 mole) of 4-p-t-butylphenoxy-1-butanol dissolved in 400 ml of dichloromethane. After forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate. The dichloromethane solution was dried over magnesium sulfate and evaporated to a syrupy residue. The material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4, to afford 43.8 g (45%) of the nicotinate ester as an oil. The hydrobromide salt was prepared by treatment of a solution of 43.8 g in 800 ml of ethyl acetate with 30 ml of 4.5N hydrogen bromide in ether. The precipitate was collected, washed with pentane and dried, m.p. 132°-133° C.

후처리

  1. temperatureat reflux for two hours
  2. customThe excess thionyl chloride was removed in vacuo
  3. washAfter forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate
  4. dry with materialThe dichloromethane solution was dried over magnesium sulfate
  5. customevaporated to a syrupy residue
  6. customThe material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4

출처 및 근거

ORD 기록
ord-d238f04b14bc48fe99e1c99449a0250c
출처 데이터셋
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05242936

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트