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

Lactic Acid → 4-Methoxybenzyl 2-hydroxypropionate

HRID 488996
노트
인쇄 미리보기

반응식

HRID 488996 반응식
[OH:1][CH:2]([CH3:6])[C:3]([OH:5])=[O:4].CC(C)([O-])C.[K+].[CH3:13][O:14][C:15]1[CH:22]=[CH:21][C:18]([CH2:19]Cl)=[CH:17][CH:16]=1>CN(C=O)C>[OH:1][CH:2]([CH3:6])[C:3]([O:5][CH2:19][C:18]1[CH:21]=[CH:22][C:15]([O:14][CH3:13])=[CH:16][CH:17]=1)=[O:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 612Lactic AcidHCID 699934-Methyloxybenzyl chlorideHCID 23665647Potassium tert-butoxide

생성물 1

HCID 220357644-Methoxybenzyl 2-hydroxypropionate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
60 °C

실험 절차

To a stirred solution of DL-2 hydroxypropionic acid (9.0 g, 100 mmole) in 100 ml dry DMF was added potassium tert-butoxide (12.34 g, 110 mmole) and the mixture was stirred for one hour at 60° C. 4-methoxybenzyl chloride (18.8 g 120 mmole) was added and the mixture was stirred for eight hours at 60° C. The mixture was evaporated under reduced pressure and 250 ml ethyl acatate was added. The organic phase was washed four times with water. The organic phase was dried with sodium sulfate and concentrated in vacuo. Yield: 16.8 g

후처리

  1. stirringthe mixture was stirred for eight hours at 60° C
  2. customThe mixture was evaporated under reduced pressure and 250 ml ethyl acatate
  3. additionwas added
  4. washThe organic phase was washed four times with water
  5. dry with materialThe organic phase was dried with sodium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-11bce5b0c8364ad5ac2083fc46e33287
출처 데이터셋
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06974802B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트