HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712148Generated: October 29, 2026
Benzoyl isothiocyanate → N-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamide
https://huagongshe.com/reaction/712148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 3-(Benzyloxy)-5-bromoaniline | HCID 57813626 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamide | HCID 57813640 | 85% |
Reaction Steps
To a solution of 3-benzyloxy-5-bromo-aniline (480 g, 1.73 mol) in acetone (10 L) was added benzoylisothiocyanate (280 mL, 2.08 mol) at rt. After stirring the reaction mixture for 15 min, solid precipitated out and stirring was continued for 30 min at rt. After completion of reaction (by TLC), acetone was distilled off. Hexane (2 L) was added and again concentrated. To the concentrated solid was added hexane (4 L) heated to 40° C. for 30 min under stirring and the solid filtered. The solid was washed with hexane (2×2 L) to obtain the desired product (648 g, 85%).
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-42d1b256812e4f4bb9a9e690709e631a |
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| Source note | uspto-grants-2015_11 |
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