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

Acetic Acid → HCID 178434812, 화합물

HRID 1903153
노트
인쇄 미리보기

반응식

HRID 1903153 반응식
Cl.Cl.[CH3:3][CH:4]1[O:8][C:7]2[CH:9]=[C:10]([NH2:14])[C:11]([NH2:13])=[CH:12][C:6]=2[O:5]1.[OH-].[K+].C(O[C:20]([S-])=[S:21])C.[K+].C(O)(=O)C>C(O)(C)C.O>[CH3:3][CH:4]1[O:5][C:6]2=[CH:12][C:11]3[NH:13][C:20]([SH:21])=[N:14][C:10]=3[CH:9]=[C:7]2[O:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 14797Potassium HydroxideHCID 2735045Potassium ethylxanthateHCID 233138062-Methyl-1,3-benzodioxole-5,6-diamine dihydrochloride

생성물 1

HCID 178434812HCID 178434812, 화합물수율 87.4%

시약·촉매·용매 2

HCID 962Water용매2회
HCID 3776Isopropanol용매

실험 절차

9.9 g of 2-methyl-1,3-benzodioxole-5,6-diamine dihydrochloride were suspended in 125 ml of isopropanol. While stirring there was added dropwise thereto a solution of 4.75 g of potassium hydroxide in 40 ml of water and the mixture was stirred at room temperature for an additional 30 minutes. After adding 7.5 g of purified potassium ethylxanthate, the solution was boiled at reflux overnight, then diluted with 125 ml of water and made neutral with a small amount of glacial acetic acid. The cooled suspension was filtered under suction and the crystals were washed well with water. There were obtained 7.5 g (87.4% of theory) of 2-methyl-5H-1,3-dioxolo(4,5-f)benzimidazole-6-thiol with a melting point above 300° C.

후처리

  1. additionwas added dropwise
  2. temperatureat reflux overnight
  3. filtrationThe cooled suspension was filtered under suction
  4. washthe crystals were washed well with water

출처 및 근거

ORD 기록
ord-63a4f3c75c9645cf8906a7f493867372
출처 데이터셋
uspto-grants-1984_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04435406

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트