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Hydrochloric Acid → (3-Acetoxy-4-nitro-phenyl)acetic acid

HRID 49714
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HRID 49714 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH2:11][C:12]([OH:14])=[O:13])[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9].[OH-].[Na+].[C:17](OC(=O)C)(=[O:19])[CH3:18].Cl>C(OCC)C>[C:17]([O:1][C:2]1[CH:3]=[C:4]([CH2:11][C:12]([OH:14])=[O:13])[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9])(=[O:19])[CH3:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 7918Acetic AnhydrideHCID 14798Sodium HydroxideHCID 235083252-(3-Hydroxy-4-nitrophenyl)acetic acid

생성물 1

HCID 17946639(3-Acetoxy-4-nitro-phenyl)acetic acid수율 519.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether
용매

반응 조건

온도
0 °C

실험 절차

A stirred mixture of (3-hydroxy-4-nitro-phenyl)acetic acid (1 2.0 g), aqueous sodium hydroxide (152.3 mL, 1M) and diethyl ether (150 mL), cooled to 0° C. in an ice salt bath, was treated dropwise with acetic anhydride (8.1 g) at a rate to maintain the temperature at 0° C. When the addition was complete the mixture was stirred at 0° C. for a further 2 hours then acidified with dilute hydrochloric acid and then extracted with ethyl acetate. The extracts were dried over magnesium sulphate and then evaporated to give the title compound (12.6 g) as an oil.

후처리

  1. temperatureto maintain the temperature at 0° C
  2. additionWhen the addition
  3. extractionextracted with ethyl acetate
  4. dry with materialThe extracts were dried over magnesium sulphate
  5. customevaporated

출처 및 근거

ORD 기록
ord-60d046c6b3554acfb33ad147ac87161e
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706738B2

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