HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712188Generated: October 30, 2026
Ethyl isothiocyanatoformate → Ethyl N-[(2,3,5-tribromo-4-methoxy-phenyl)carbamothioyl]carbamate
https://huagongshe.com/reaction/712188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isothiocyanatoformate | HCID 85320 | — |
| Reactant | 2,3,5-Tribromo-4-methoxy-aniline | HCID 13399551 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl N-[(2,3,5-tribromo-4-methoxy-phenyl)carbamothioyl]carbamate | HCID 86663965 | — |
Reaction Steps
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]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181234B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-b3d82cd6133946ccb3a23b2a34cff912 |
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| Source note | uspto-grants-2015_11 |
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