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

Hydrochloric Acid → 4-(3-Bromobenzyl)-5-methylthiazole-2-carboxylic acid

HRID 517553
노트
인쇄 미리보기

반응식

HRID 517553 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][CH:19]=1)[CH2:5][C:6]1[N:7]=[C:8]([C:12]([O:14]CC)=[O:13])[S:9][C:10]=1[CH3:11].O[Li].O.Cl>C1COCC1.CO.O.CCOC(C)=O.O>[Br:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][CH:19]=1)[CH2:5][C:6]1[N:7]=[C:8]([C:12]([OH:14])=[O:13])[S:9][C:10]=1[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 313Hydrochloric AcidHCID 168937Lithium hydroxide, monohydrateHCID 86711493Ethyl 4-(3-bromobenzyl)-5-methylthiazole-2-carboxylate

생성물 1

HCID 867114944-(3-Bromobenzyl)-5-methylthiazole-2-carboxylic acid

시약·촉매·용매 3

HCID 962Water용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of ethyl 4-(3-bromobenzyl)-5-methylthiazole-2-carboxylate (20 mg, 0.06 mmol) was treated with LiOH.H2O (7.5 mg, 0.18 mmol) in 2 mL of THF/MeOH/H2O (2:1:1) and stirred at RT for 2 h. The reaction was diluted with EtOAc and H2O and then acidified by 6N HCl. The organic layer was separated and concentrated to give a crude which was used in the next step without further purification.

후처리

  1. customThe organic layer was separated
  2. concentrationconcentrated
  3. customto give a crude which
  4. customwas used in the next step without further purification

출처 및 근거

ORD 기록
ord-1bcc059b980245e1a5ec5e309f855f0a
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115120B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 21892291
Methanol tetrahydrofuran water
용매