Potassium Iodide → 5-Chloro-2-propoxybenzamide

HRID 1532087

반응식

HRID 1532087 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([CH:10]=1)[C:7]([NH2:9])=[O:8].Br[CH2:13][CH2:14][CH3:15].[I-].[K+].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:11][CH2:13][CH2:14][CH3:15])=[C:6]([CH:10]=1)[C:7]([NH2:9])=[O:8]

참가 물질

6

반응물 4

HCID 4875Potassium IodideHCID 78401-BromopropaneHCID 11430Potassium CarbonateHCID 3480945-Chloro-2-hydroxybenzamide

생성물 1

HCID 94528845-Chloro-2-propoxybenzamide

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A stirred mixture of 5-chloro-2-hydroxybenzamide (20 g), 1-bromopropane (13.4 ml), potassium iodide (2.49 g) and anhydrous potassium carbonate (24.15 g) in acetone (250 ml) was heated under reflux for 20 hours. The cooled reaction mixture was filtered and the filter cake was washed with acetone. The filtrate and washings were combined and evaporated under reduced pressure to yield a residue which was washed with water, dilute aqueous sodium hydroxide, water and with diethyl ether to yield a crude product (19.85 g). This was recrystallised from acetonitrile, partitioned between chloroform and dilute aqueous sodium hydroxide, and was recrystallised from ethanol to yield 5-chloro-2-propoxybenzamide (16.78 g).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 20 hours
  3. customThe cooled reaction mixture
  4. filtrationwas filtered
  5. washthe filter cake was washed with acetone
  6. customevaporated under reduced pressure
  7. customto yield a residue which
  8. washwas washed with water, dilute aqueous sodium hydroxide, water and with diethyl ether
  9. customto yield a crude product (19.85 g)
  10. customThis was recrystallised from acetonitrile
  11. custompartitioned between chloroform and dilute aqueous sodium hydroxide
  12. customwas recrystallised from ethanol

출처 및 근거

ORD 기록
ord-275245fa3d934c7ba5b37496525bec4c
출처 데이터셋
uspto-grants-2001_03
특허 번호
US06200980B1

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