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

Sodium Hydroxide → 6-(Cyclohexyloxy)pyrimidine-4-carboxylic acid

HRID 1746673
노트
인쇄 미리보기

반응식

HRID 1746673 반응식
[CH:1]1([O:7][C:8]2[N:13]=[CH:12][N:11]=[C:10]([C:14]([O:16]C3CCCCC3)=[O:15])[CH:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[OH-].[Na+]>C1COCC1.CCO.O>[CH:1]1([O:7][C:8]2[N:13]=[CH:12][N:11]=[C:10]([C:14]([OH:16])=[O:15])[CH:9]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 59446917Cyclohexyl 6-(cyclohexyloxy)pyrimidine-4-carboxylate

생성물 1

HCID 594470626-(Cyclohexyloxy)pyrimidine-4-carboxylic acid

시약·촉매·용매 1

HCID 18504229Ethanol tetrahydrofuran water용매

실험 절차

A solution of cyclohexyl 6-(cyclohexyloxy)pyrimidine-4-carboxylate (2.00 g; 6.57 mmol) in THF/EtOH/H2O (3/2/1, total volume 200 mL) was treated with a 5N solution of sodium hydroxide (3.94 ml; 19.7 mmol). The reaction mixture was stirred at room temperature for 2 h. The mixture was concentrated under vacuum and then water was added. The aqueous layer was washed with DCM then acidified to pH 5 by addition of 1N HCl solution. The aqueous layer was washed with EtOAc (150 mL), then lyophilized and the obtained solid was washed with DCM. The suspension was filtered off and the filtrate was concentrated under vacuum to afford the title compound as a beige solid.

후처리

  1. concentrationThe mixture was concentrated under vacuum
  2. additionwater was added
  3. washThe aqueous layer was washed with DCM
  4. additionthen acidified to pH 5 by addition of 1N HCl solution
  5. washThe aqueous layer was washed with EtOAc (150 mL)
  6. washthe obtained solid was washed with DCM
  7. filtrationThe suspension was filtered off
  8. concentrationthe filtrate was concentrated under vacuum

출처 및 근거

ORD 기록
ord-aae3ae94e79543998ee99fb745877637
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150519B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트