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

Potassium thiocyanate → (2,2-Dichloro-3,3-dimethylcyclopropyl)methyl thiocyanate

HRID 1981332
노트
인쇄 미리보기

반응식

HRID 1981332 반응식
[Cl:1][C:2]1([Cl:9])[C:4]([CH3:6])([CH3:5])[CH:3]1[CH2:7]Cl.[S-:10][C:11]#[N:12].[K+]>C(O)C>[Cl:1][C:2]1([Cl:9])[C:4]([CH3:6])([CH3:5])[CH:3]1[CH2:7][S:10][C:11]#[N:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 516872Potassium thiocyanateHCID 27752731,1-Dichloro-3-(chloromethyl)-2,2-dimethylcyclopropane

생성물 1

HCID 13313519(2,2-Dichloro-3,3-dimethylcyclopropyl)methyl thiocyanate수율 85.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

1.87 g of 2,2-dichloro-3,3-dimethyl-1-chloromethylcyclopropane and 1.0 g of potassium thiocyanate were suspended in 20 ml of ethanol, and the suspension was refluxed for 12 hours. Ethanol was evaporated, and 20 ml of water was added. The mixture was extracted with toluene. The toluene layer was washed with water and dried over sodium sulfate. The toluene was then evaporated under reduced pressure to give 1.80 g of 2,2-dichloro-3,3-dimethylcyclopropylmethyl thiocyanate, the desired compound shown above. The boiling point of the product was 115° C. at 200 mmHg.

후처리

  1. temperaturethe suspension was refluxed for 12 hours
  2. customEthanol was evaporated
  3. addition20 ml of water was added
  4. extractionThe mixture was extracted with toluene
  5. washThe toluene layer was washed with water
  6. dry with materialdried over sodium sulfate
  7. customThe toluene was then evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-b3a5eab249d44e83841cdbc99e247a0d
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04514418

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트