Ethyl isothiocyanatoformate → Ethyl N-[(2,3,5-tribromo-4-methoxy-phenyl)carbamothioyl]carbamate

HRID 712188노트

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HRID 712188 반응식
[Br:1][C:2]1[C:8]([Br:9])=[C:7]([O:10][CH3:11])[C:6]([Br:12])=[CH:5][C:3]=1[NH2:4].[CH2:13]([O:15][C:16]([N:18]=[C:19]=[S:20])=[O:17])[CH3:14]>CC(C)=O>[Br:1][C:2]1[C:8]([Br:9])=[C:7]([O:10][CH3:11])[C:6]([Br:12])=[CH:5][C:3]=1[NH:4][C:19]([NH:18][C:16](=[O:17])[O:15][CH2:13][CH3:14])=[S:20]

참가 물질

4

반응물 2

HCID 85320Ethyl isothiocyanatoformateHCID 133995512,3,5-Tribromo-4-methoxy-aniline

생성물 1

HCID 86663965Ethyl N-[(2,3,5-tribromo-4-methoxy-phenyl)carbamothioyl]carbamate

시약·촉매·용매 1

HCID 180Acetone용매

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온도
40 °C

실험 절차

2,3,5-Tribromo-4-methoxy-aniline (4.72 g, 13.1 mmol) was dissolved in acetone (150 mL) and ethoxycarbonyl isothiocyanate (1.63 mL, 14.4 mmol) was added. The solution was heated to 40° C. After 20 minutes a pale yellow precipitate had formed. The viscous mixture was cooled to rt and stirred at rt overnight. The solvent was removed under reduced pressure. Cyclohexane (˜150 mL) was added to the residue and the suspension sonicated. The solid was collected by filtration through a PTFE filter to give an off-white fluffy solid which was dried in the vacuum oven (40° C.) to afford the desired compound as an off-white solid, 6.00 g (93%). m/z: 488.78/490.80/492.75/494.80 [M+H]+.

후처리

  1. customAfter 20 minutes a pale yellow precipitate had formed
  2. temperatureThe viscous mixture was cooled to rt
  3. customThe solvent was removed under reduced pressure
  4. additionCyclohexane (˜150 mL) was added to the residue
  5. customthe suspension sonicated
  6. filtrationThe solid was collected by filtration through a PTFE
  7. filtrationfilter
  8. customto give an off-white fluffy solid which
  9. customwas dried in the vacuum oven (40° C.)

출처 및 근거

ORD 기록
ord-b3d82cd6133946ccb3a23b2a34cff912
출처 데이터셋
uspto-grants-2015_11
특허 번호
US09181234B2

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