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Benzaldehyde → Hydrobenzamide

HRID 1608560
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HRID 1608560 반응식
[NH4+:1].[OH-].[CH:3](=O)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>CC(O)C>[CH:7]1[CH:8]=[CH:9][C:4](/[CH:3]=[N:1]/[CH:3]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)/[N:1]=[CH:3]/[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 240BenzaldehydeHCID 14923Ammonium Hydroxide

생성물 1

HCID 9566477Hydrobenzamide수율 97.5%

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a 3 L 3-necked flask equipped with a mechanical stirrer and a thermometer was added 1 L of concentrated NH4OH (ca 30%) (14.8 moles). A solution of benzaldehyde (265 g, 2.50 mol) in 500 mL of 2-propanol was added in one portion. The mixture was stirred vigorously at ca 22° C. for 43 hours. The resulting slurry was filtered and the filter cake was washed with water (1 L). After drying in vacuo, 242.4 g of hydrobenzamide was obtained as a white solid (mp 100°-102° C.) for a 97.4% yield.

후처리

  1. customTo a 3 L 3-necked flask equipped with a mechanical stirrer
  2. filtrationThe resulting slurry was filtered
  3. washthe filter cake was washed with water (1 L)
  4. customAfter drying in vacuo

출처 및 근거

ORD 기록
ord-46091f7cc8d24bd09b1071ef54d6f8fa
출처 데이터셋
uspto-grants-1995_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05395850

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