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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2-Chloro-N-(2,5-dihydroxy-phenyl)-acetamide

HRID 280820
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HRID 280820 반응식
[Cl:1][CH2:2][C:3](Cl)=[O:4].[NH2:6][C:7]1[CH:13]=[C:12]([OH:14])[CH:11]=[CH:10][C:8]=1[OH:9].N(CCO)CCO.Cl>CC(C)=O.O>[Cl:1][CH2:2][C:3]([NH:6][C:7]1[CH:13]=[C:12]([OH:14])[CH:11]=[CH:10][C:8]=1[OH:9])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 6577Chloroacetyl chlorideHCID 8113DiethanolamineHCID 3017497Aminohydroquinone

생성물 1

HCID 212986772-Chloro-N-(2,5-dihydroxy-phenyl)-acetamide

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매

실험 절차

α-chloroacetylchloride (10.1 g, 0.128 mole) was added dropwise under stirring at room temperature to the 2-aminohydroquinone (4.16 g, 0.128 mole) in dry acetone (400 ml) and diethanolamine (2.04 ml, 0.128 mole). The reaction mixture was poured into water and hydrochloride acid (2,000 ml, pH 1), then extracted with ethylacetate (500 ml). The solvent was evaporated to dryness and the solid residue (4.20 g, 80%) was used without any further purification. The structure of the 2-(α-chloroacetamido)-hydroquinone was confirmed by NMR analysis.

후처리

  1. extractionextracted with ethylacetate (500 ml)
  2. customThe solvent was evaporated to dryness
  3. customthe solid residue (4.20 g, 80%) was used without any further purification

출처 및 근거

ORD 기록
ord-0984854f25914b0bae7e4123b8e452e8
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04591548

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