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

Sodium Cyanide → 8-t-Butyl-3-cyano-1-oxaspiro(4,5)decane

HRID 1684684
노트
인쇄 미리보기

반응식

HRID 1684684 반응식
[C:1]([CH:5]1[CH2:25][CH2:24][C:8]2([O:12][CH2:11][CH:10](OS(C3C=CC(C)=CC=3)(=O)=O)[CH2:9]2)[CH2:7][CH2:6]1)([CH3:4])([CH3:3])[CH3:2].[C-:26]#[N:27].[Na+]>CN(C=O)C>[C:1]([CH:5]1[CH2:6][CH2:7][C:8]2([O:12][CH2:11][CH:10]([C:26]#[N:27])[CH2:9]2)[CH2:24][CH2:25]1)([CH3:2])([CH3:3])[CH3:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8929Sodium CyanideHCID 190401668-t-Butyl-3-(p-toluenesulfonyloxy)-1-oxaspiro-(4,5)decane

생성물 1

HCID 190401648-t-Butyl-3-cyano-1-oxaspiro(4,5)decane수율 99.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
100 °C

실험 절차

A mixture of 8-t-butyl-3-(p-toluenesulfonyloxy)-1-oxaspiro-(4,5)decane (18.3 g, 50 mmol) and sodium cyanide (4.9 g, 100 mmol) in dry DMF (75 ml) was heated to 100° C. for 6 hours. Light petroleum/ethylacetate 4:1 (50 ml) was added and the mixture was filtrated from insoluble material. The filtrate was then evaporated in vacuo and the resulting residue was taken up in toluene (100 ml). It was washed with water, dried (MgSO4) and evaporated in vacuo to yield a brownish oil (11.0 g) which was Kugelrohr distilled (120°-125° C., 0.015 mbar) to furnish the product as colourless crystals (8.94 g, m.p. 35°-40° C.).

후처리

  1. filtrationthe mixture was filtrated from insoluble material
  2. customThe filtrate was then evaporated in vacuo
  3. washIt was washed with water
  4. dry with materialdried (MgSO4)
  5. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-97ad4a7846574fea9e5e3e3c9eece48a
출처 데이터셋
uspto-grants-1997_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05641883

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트