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

Potassium Cyanide → HCID 54047757, 화합물

HRID 1388115
노트
인쇄 미리보기

반응식

HRID 1388115 반응식
S(=O)(O)[O-].[Na+].[CH3:6][C@@H:7]1[CH:12]=[CH:11][CH2:10][CH2:9][C@H:8]1[CH:13]=[O:14].[C-:15]#[N:16].[K+]>O.C(O)C>[CH3:6][C@@H:7]1[CH:12]=[CH:11][CH2:10][CH2:9][C@H:8]1[CH:13]([OH:14])[C:15]#[N:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 9032Potassium CyanideHCID 12613984(1R,2R)-2-Methylcyclohex-3-ene-1-carbaldehydeHCID 23665763Sodium Bisulfite

생성물 1

HCID 54047757HCID 54047757, 화합물

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

반응 조건

온도
15 °C

실험 절차

Sodium bisulfite (10.4 g., 0.1 mole) was dissolved in 50 ml. H2O. Absolute ethanol (50 ml.) and trans-2-methyl-3-cyclohexene-1-carbaldehyde (85%, 8.6 g., 0.07 mole) were added and the mixture heated in an oil bath at 63°-65° C. for 1.5 hours, then cooled to 15° C. in an ice-water bath. KCN (13 g., 0.2 mole) in 50 ml. H2O was added at 15°-18° C. The reaction mixture was stirred at room temperature 0.5 hour and extracted with 150 ml. ether. The ether was back-washed with 75 ml. H2O and concentrated in vacuo to yield title product as an oil, 5.5 g. Based on pnmr, the product contained 85% trans isomer (doublet at 4.6 ppm, J=4) and 15% cis isomer (doublets at 4.2 and 4.35, J=2).

후처리

  1. temperaturethe mixture heated in an oil bath at 63°-65° C. for 1.5 hours
  2. extractionextracted with 150 ml
  3. washThe ether was back-washed with 75 ml
  4. concentrationH2O and concentrated in vacuo

출처 및 근거

ORD 기록
ord-0e0fa6b974684baaa2f218cfef55c79c
출처 데이터셋
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04430337

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트