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

Water → 2-Methyl-4-(p-tolyl)thiazole-5-carboxylic acid

HRID 883633
노트
인쇄 미리보기

반응식

HRID 883633 반응식
C[O:2][C:3]([C:5]1[S:9][C:8]([CH3:10])=[N:7][C:6]=1[C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=1)=[O:4].[OH-].[K+].O>C(O)C>[CH3:10][C:8]1[S:9][C:5]([C:3]([OH:4])=[O:2])=[C:6]([C:11]2[CH:12]=[CH:13][C:14]([CH3:17])=[CH:15][CH:16]=2)[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14797Potassium HydroxideHCID 670181442-Methyl-4-p-tolyl-thiazole-5-carboxylic acid methyl ester

생성물 1

HCID 588288142-Methyl-4-(p-tolyl)thiazole-5-carboxylic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2-Methyl-4-p-tolyl-thiazole-5-carboxylic acid methyl ester (2.67 mmol) and solid KOH (5.35 mmol) were dissolved in ethanol (1.04 mL) and water (0.26 mL) and heated under reflux for 3 hours. After cooling, the solvent was evaporated under reduced pressure and ice water was added to the residue, followed by washing with hexane. The aqueous layer was acidified with 1N aq. HCl and the crystals thus precipitated were collected by filtration, washed with water and then dried to provide 2-methyl-4-p-tolyl-thiazole-5-carboxylic acid. LC-MS: tR=0.83 min; [m+H]+=234.02.

후처리

  1. temperatureunder reflux for 3 hours
  2. temperatureAfter cooling
  3. customthe solvent was evaporated under reduced pressure and ice water
  4. additionwas added to the residue
  5. washby washing with hexane
  6. customthe crystals thus precipitated
  7. filtrationwere collected by filtration
  8. washwashed with water
  9. customdried

출처 및 근거

ORD 기록
ord-a066f531451a46efa0956209ac26f940
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08236964B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트