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Dimethylhydantoin → 3-(6-Chloro-n-hexyl)-5,5-dimethyl-hydantoin

HRID 2071593
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인쇄 미리보기

반응식

HRID 2071593 반응식
[CH3:1][C:2]1([CH3:9])[NH:6][C:5](=[O:7])[NH:4][C:3]1=[O:8].C(=O)([O-])[O-].[K+].[K+].[Cl:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]Cl>O>[Cl:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][N:4]1[C:3](=[O:8])[C:2]([CH3:9])([CH3:1])[NH:6][C:5]1=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6491DimethylhydantoinHCID 11430Potassium CarbonateHCID 165511,6-Dichlorohexane

생성물 1

HCID 214116503-(6-Chloro-n-hexyl)-5,5-dimethyl-hydantoin

시약·촉매·용매 1

HCID 962Water용매

실험 절차

128 g of 5,5-dimethyl-hydantoin (1.0 mol), 69 g of anhydrous potassium carbonate (0.5 mol) and 775 g of 1,6-dichlorohexane are reacted at 132°-150° C internal temperature (external temperature 160° C) and the resulting water of reaction is removed continuously by azeotropic circulatory distillation. After 6 hours 25 minutes, the reaction is complete and the reaction mixture is filtered hot to remove the potassium chloride formed. The filtrate is concentrated on a rotary evaporator and dried to constant weight at 100° C and 10-1 mm Hg.

후처리

  1. customis removed continuously by azeotropic circulatory distillation
  2. filtrationthe reaction mixture is filtered hot
  3. customto remove the potassium chloride
  4. customformed
  5. concentrationThe filtrate is concentrated on a rotary evaporator
  6. customdried to constant weight at 100° C

출처 및 근거

ORD 기록
ord-5dde6db7407342d185044f30073d73f9
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04048170

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