Water → HCID 53897658, 화합물

HRID 342752노트

반응식

HRID 342752 반응식
[CH3:1][C:2]([NH:8][C:9](=[O:18])[C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([Cl:17])[CH:11]=1)([CH3:7])[C:3]([CH2:5]Cl)=[O:4].[C:19]([O-:22])(=[O:21])[CH3:20].[Na+].O>CN(C=O)C>[CH3:1][C:2]([NH:8][C:9](=[O:18])[C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([Cl:17])[CH:11]=1)([CH3:7])[C:3]([CH2:5][O:22][C:19](=[O:21])[CH3:20])=[O:4]

참가 물질

5

반응물 3

HCID 962WaterHCID 517045Sodium AcetateHCID 54029353HCID 54029353, 화합물

생성물 1

HCID 53897658HCID 53897658, 화합물수율 47.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

N-(1',1'-dimethyl-3'-chloroacetonyl)-3,5-dichlorobenzamide (20 gm, 0.065 m) was dissolved in 100 ml of dry DMF and 10.6 gm (0.128 m) of sodium acetate was added. The slurry was blanketed under a nitrogen atmosphere and then heated to 80°-90° C. for 4 days. The reaction mixture was cooled by adding 100 ml of water. The aqueous solution was extracted four times with 10 ml aliquots of methylene chloride. The combined organic extracts were washed with water (3×100 ml) and brine. The solvent was removed, the resulting white solid dried and then recrystallized from an acetone and hexane (about 1:4) mixture to yield 10.2 gm of the product.

후처리

  1. temperatureheated to 80°-90° C. for 4 days
  2. temperatureThe reaction mixture was cooled
  3. extractionThe aqueous solution was extracted four times with 10 ml aliquots of methylene chloride
  4. washThe combined organic extracts were washed with water (3×100 ml) and brine
  5. customThe solvent was removed
  6. customthe resulting white solid dried
  7. customrecrystallized from an acetone and hexane (about 1:4) mixture

출처 및 근거

ORD 기록
ord-f19ab130800a4b1d90ff51182f3c0aed
출처 데이터셋
uspto-grants-1999_01
특허 번호
US05859063

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