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

1-Bromohexane → Sbb043676

HRID 1252091
노트
인쇄 미리보기

반응식

HRID 1252091 반응식
[NH2:1][C:2]1[S:3][C:4]([SH:7])=[N:5][N:6]=1.[OH-].[Na+].Br[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>O.C(O)C>[NH2:1][C:2]1[S:3][C:4]([S:7][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[N:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 81011-BromohexaneHCID 14798Sodium HydroxideHCID 178509208HCID 178509208, 화합물

생성물 1

HCID 1579472Sbb043676수율 78.7%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

실험 절차

In 24 ml of water and 24 ml of ethanol, 11.6 g of 2-amino-5-mercapto-1,3,4-thiadiazole and 3.8 g of sodium hydroxide were dissolved, 14.0 g of 1-bromohexane was added to this solution, and the mixture was heated to 70°-80° C. and stirred for 3 hours. After cooling, water was added and the mixture was filtered. The residue was washed with water, dried under reduced pressure, and recrystallized from an ethanol/n-hexane (1:1) mixture. Thus 14.5 g of 2-amino-5-hexylthio-1,3,4-thiadiazole was obtained. m.p. 113°-115° C. Yield 77%.

후처리

  1. temperaturethe mixture was heated to 70°-80° C.
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. washThe residue was washed with water
  5. customdried under reduced pressure
  6. customrecrystallized from an ethanol/n-hexane (1:1) mixture

출처 및 근거

ORD 기록
ord-6432914c090d4f8787e299adb34c0060
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04742063

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트