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

Hydrochloric Acid → 4-Propylhept-1-en-4-ol

HRID 249061
노트
인쇄 미리보기

반응식

HRID 249061 반응식
[CH3:1][CH2:2][CH2:3][C:4](=[O:8])[CH2:5][CH2:6][CH3:7].[CH2:9]([Mg]Br)[CH:10]=[CH2:11].C(Br)C=C.[NH4+].[Cl-].Cl>C(OCC)C>[OH:8][C:4]([CH2:9][CH2:10][CH3:11])([CH2:5][CH2:6][CH3:7])[CH2:3][CH:2]=[CH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 7841Allyl bromideHCID 25517Ammonium ChlorideHCID 312464-HeptanoneHCID 178455850HCID 178455850, 화합물

생성물 1

HCID 5513824-Propylhept-1-en-4-ol

시약·촉매·용매 1

HCID 3283Diethyl Ether

실험 절차

113 g of 4-heptanone in 1000 ml of dry diethyl ether was slowly added to a solution of allylmagnesium bromide, prepared from 36.5 g of Mg and 178 g of allyl bromide in 500 ml dry diethyl ether. After the addition the mixture was refluxed for 10 hrs. The reaction mixture was poured on a mixture of 150 g ice, 450 ml of 20% NH4Cl and 350 ml of 5M HCl. The ether phase was separated and the water phase extracted with diethyl ether (3×100 ml). The combined organic phases were then washed with a Na2CO3 -solution and water, dried with Na2SO4 and evaporated. The residue was distilled. Yield: 142 g (b.p. 38°-40° C./0.1 torr)

후처리

  1. additionAfter the addition the mixture
  2. temperaturewas refluxed for 10 hrs
  3. customThe ether phase was separated
  4. extractionthe water phase extracted with diethyl ether (3×100 ml)
  5. washThe combined organic phases were then washed with a Na2CO3 -solution and water
  6. dry with materialdried with Na2SO4
  7. customevaporated
  8. distillationThe residue was distilled

출처 및 근거

ORD 기록
ord-0e01eb8edbf44983986d69a0faa08a22
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05212305

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
용매
2회