Sodium Hydroxide → Sodium 2-amino-3-benzoyl-alpha-methylphenylacetate Hydrate

HRID 442553

반응식

HRID 442553 반응식
[C:1]([C:9]1[CH:10]=[CH:11][CH:12]=[C:13]2[C:17]=1[NH:16][C:15](=[O:18])[CH:14]2[CH3:19])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-:20].[Na+:21]>O>[OH2:8].[NH2:16][C:17]1[C:9]([C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:10][CH:11]=[CH:12][C:13]=1[CH:14]([CH3:19])[C:15]([O-:20])=[O:18].[Na+:21]

참가 물질

4

반응물 2

HCID 14798Sodium Hydroxide2회HCID 129012437-Benzoyl-3-methyl-1,3-dihydro-2H-indol-2-one

생성물 1

HCID 70591625Sodium 2-amino-3-benzoyl-alpha-methylphenylacetate Hydrate

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A suspension of 9 g. (0.036 mole) of 7-benzoyl-3-methylindolin-2-one in 100 ml. of 3N sodium hydroxide was refluxed for 18 hrs. under nitrogen. The mixture was filtered and stripped under water pump vacuum to yield a gummy mixture of sodium hydroxide, water, and product. The mixture was triturated with boiling isopropanol and filtered. The isopropanol solution was cooled and filtered to separate the bright yellow product. The product weighed 4.0 g. and melted at 218° C. (dec.)

후처리

  1. additionA suspension of 9 g
  2. filtrationThe mixture was filtered
  3. customto yield
  4. customThe mixture was triturated with boiling isopropanol
  5. filtrationfiltered
  6. temperatureThe isopropanol solution was cooled
  7. filtrationfiltered
  8. customto separate the bright yellow product

출처 및 근거

ORD 기록
ord-6763f917c09b4e4bbd1a9ceb3e1d99ed
출처 데이터셋
uspto-grants-1977_08
특허 번호
US04045576

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