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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → [4-(Methylamino)phenyl]acetic acid

HRID 507500
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인쇄 미리보기

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HRID 507500 반응식
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([O:12]C)=[O:11])=[CH:5][CH:4]=1.[OH-].[Li+].Cl>O1CCCC1>[CH3:1][NH:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:9][C:10]([OH:12])=[O:11])=[CH:7][CH:8]=1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 15892780Methyl 2-(4-(methylamino)phenyl)acetate

생성물 1

HCID 290114[4-(Methylamino)phenyl]acetic acid수율 46.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 2-(4-(methylamino)phenyl)acetate (721 mg. 4.0 mmol) was dissolved in tetrahydrofuran (10 mL) and treated with a 1 M aqueous solution of lithium hydroxide (4.4 mmol). After 3 hours, the mixture was acidified with 1 N aqueous hydrochloric acid and concentrated to remove tetrahydrofuran. The aqueous phase was extracted with dichloromethane (2×20 mL) and the organic layer was dried and concentrated to give 2-(4-(methylamino)phenyl)acetic acid (309 mg, 1.87 mmol).

후처리

  1. concentrationconcentrated
  2. customto remove tetrahydrofuran
  3. extractionThe aqueous phase was extracted with dichloromethane (2×20 mL)
  4. customthe organic layer was dried
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e8d93139095f4edeba40ffc9ad2da402
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07786171B2

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