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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → (4-Amino-3-bromophenyl)acetic acid

HRID 1733018
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인쇄 미리보기

반응식

HRID 1733018 반응식
C([NH:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=[O:13])=[CH:7][C:6]=1[Br:15])(=O)C.[OH-].[Na+].C(O)(=O)C>Cl>[NH2:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=[O:13])=[CH:7][C:6]=1[Br:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 203034124-(Acetylamino)-3-bromobenzeneacetic acid

생성물 1

HCID 20303490(4-Amino-3-bromophenyl)acetic acid수율 91.4%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

30.5 g (0.112 mole) of 4-acetamido-3-bromophenylacetic acid are heated to 100° C. in 100 ml of 6 N hydrochloric acid until a clear solution forms, and the mixture is subsequently kept at 110° C. for one hour. Cooling is effected, followed by rendering alkaline with a solution of sodium hydroxide and acidifying with glacial acetic acid. The thus-formed flocculent precipitate is suction filtered, washed with water and dried to obtain 23.5 g (91.4% of theory) of 4-amino-3-bromophenylacetic acid (m.p. 139° to 140° C.).

후처리

  1. temperatureCooling
  2. filtrationfiltered
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-b757cdc7c78541d7b4e2ffb8d19bb4c8
출처 데이터셋
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04239901

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