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

Hydrochloric Acid → 1H-Benzimidazole-1-butanamine

HRID 1388909
노트
인쇄 미리보기

반응식

HRID 1388909 반응식
[N:1]1([CH2:10][CH2:11][CH2:12][C:13]#[N:14])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.Cl>[Pd].C(O)C>[N:1]1([CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 130667534-(1H-Benzimidazol-1-yl)butanenitrile

생성물 1

HCID 43794811H-Benzimidazole-1-butanamine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution was prepared from 8.9 grams of the nitrile and 150 ml of absolute ethanol, 0.8 grams of palladium on charcoal and 8 ml of concentrated hydrochloric acid were added, and the resulting mixture was hydrogenated at room temperature and pressure for 48 hours. The reaction mixture was then filtered, the solvent was evaporated from the filtrate, and the residue was treated with aqueous 2 N sodium hydroxide solution and extracted with chloroform. The chloroform solution was dried and then distilled to give 1H-benzimidazole-1-butanamine boiling at about 180°-186° C. at 1.2 mm pressure.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionwere added
  2. customwas hydrogenated at room temperature
  3. filtrationThe reaction mixture was then filtered
  4. customthe solvent was evaporated from the filtrate
  5. additionthe residue was treated with aqueous 2 N sodium hydroxide solution
  6. extractionextracted with chloroform
  7. dry with materialThe chloroform solution was dried
  8. distillationdistilled

출처 및 근거

ORD 기록
ord-eafdd4da9be94c9489f644686084e4b6
출처 데이터셋
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04434174

반응 노트

불러오는 중…