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

Lithium hydroxide, monohydrate → HCID 178524764, 화합물

HRID 1953056
노트
인쇄 미리보기

반응식

HRID 1953056 반응식
O[Li].O.[OH:4][C:5]1[C:10]([C:11]([O:13]C)=[O:12])=[CH:9][N:8]=[CH:7][N:6]=1>O.O1CCCC1>[OH:4][C:5]1[C:10]([C:11]([OH:13])=[O:12])=[CH:9][N:8]=[CH:7][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 178498837HCID 178498837, 화합물

생성물 1

HCID 178524764HCID 178524764, 화합물

시약·촉매·용매 1

HCID 21881883Oxolane--water (1/1)용매

실험 절차

The moist sodium salt of methyl 4-hydroxypyrimidine-5-carboxylate obtained as in Example 2a) was taken up in water/tetrahydrofuran=1:1, and 1.0 eq of LiOH.H2O was added. Following hydrolysis of the ester over 3.5 hours at 0° C. and 2 hours at room temperature, most of the tetrahydrofuran was evaporated and, at 0° C., a pH of 3 was adjusted using eq. HCl solution. After about 45 minutes at 0° C., the title product was filtered off. Drying gave the acid in a yield of 3.55 g (78%).

후처리

  1. additionwas added
  2. custom2 hours at room temperature, most of the tetrahydrofuran was evaporated and, at 0° C.
  3. filtrationthe title product was filtered off
  4. customDrying
  5. customgave the acid in a yield of 3.55 g (78%)

출처 및 근거

ORD 기록
ord-bf7b8571eb4f4372a70f6bb8fc3b029e
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06114527

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트