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

Methyl 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylate → 7-Chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylic acid

HRID 1868356
노트
인쇄 미리보기

반응식

HRID 1868356 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:14]([O:16]C)=[O:15])[C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[C:11]=1[O:12][CH3:13]>[OH-].[Na+]>[Cl:1][C:2]1[CH:3]=[C:4]([C:14]([OH:16])=[O:15])[C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[C:11]=1[O:12][CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 11565132Methyl 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylate

생성물 1

HCID 115939517-Chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylic acid수율 2.6%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

A mixture of intermediate (2) (0.138 mol) in a 2N NaOH solution (500 ml) was stirred and refluxed for 1 hour, then cooled and washed with DCM. The mixture was separated into its layers. The aqueous layer was acidified with a concentrated HCl solution until pH=2. The solid was filtered off, washed with water and dried in vacuo. A part (2.5 g) of this fraction was crystallized from methanol. The precipitate was filtered off and dried, yielding 0.88 g of 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylic acid (intermediate 3, mp. 172° C.).

후처리

  1. temperaturerefluxed for 1 hour
  2. temperaturecooled
  3. washwashed with DCM
  4. customThe mixture was separated into its layers
  5. filtrationThe solid was filtered off
  6. washwashed with water
  7. customdried in vacuo
  8. customA part (2.5 g) of this fraction was crystallized from methanol
  9. filtrationThe precipitate was filtered off
  10. customdried

출처 및 근거

ORD 기록
ord-331ee86488bb45b8aa2398f3db7e4946
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07635706B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트