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Acetic Acid → HCID 13257633、化合物

HRID 1702119
ノート
印刷プレビュー

反応式

HRID 1702119 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:16](=[O:17])[C:15]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:9]2=[O:18])=[C:4]([F:19])[CH:3]=1.[BH4-].[Na+].C(O)(=O)C>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:16]([OH:17])[C:15]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:9]2=[O:18])=[C:4]([F:19])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 176Acetic AcidHCID 1859312-(4-Chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dioneHCID 4311764Sodium borohydride

生成物 1

HCID 13257633HCID 13257633、化合物収率 90%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

In 400 ml of ethanol was dissolved 40.0 g of 2-(4-chloro-2-fluorophenyl)-2,3,4,5,6,7-hexahydro-1H-isoindol-1,3-dione, and 2.4 g of sodium borohydride was added to the solution with stirring over a 30-minute period, while cooling was effected suitably so as to maintain the reaction temperature at 20° to 30° C. After stirring was further continued at room temperature for 1 hour, the reaction mixture was neutralized with dilute acetic acid and concentrated to about one third of the original volume, followed by cooling. The resulting crystals were collected by filtration, washed with water and dried, thereby affording 36.2 g (yield of 90%) of the subject compound. Recrystallization from ethyl acetate yielded white crystals, m.p. 178°-179° C.

後処理

  1. additionwas added to the solution
  2. temperaturewhile cooling
  3. temperatureto maintain the reaction temperature at 20° to 30° C
  4. stirringAfter stirring
  5. concentrationconcentrated to about one third of the original volume
  6. temperatureby cooling
  7. filtrationThe resulting crystals were collected by filtration
  8. washwashed with water
  9. customdried

出典と根拠

ORDレコード
ord-a93df3e1e65e471ea2a0a4b4837b7a7f
出典データセット
uspto-grants-1983_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04380466

反応ノート

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