HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447055Generated: October 30, 2026
Sodium Hydroxide → (3-Benzyloxy-5-bromo-phenyl)thiourea
https://huagongshe.com/reaction/447055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamide | HCID 57813640 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Benzyloxy-5-bromo-phenyl)thiourea | HCID 57813605 | 94% |
Reaction Steps
To an ice-cold solution of 1-benzoyl-3-(3-benzyloxy-5-bromo-phenyl)thiourea (33.0 g, 74.70 mmol) in THF (500.0 mL) was added a solution of NaOH (15.0 g, 375.0 mmol) in H2O (180.0 mL). The resulting reaction mixture was stirred at 65° C. for 15 h. The reaction mass was then cooled to room temperature, added water and extracted with EtOAc (3×1.0 L). The combined organics was washed with water, dried over anhydrous Na2SO4 and concentrated under reduced pressure to get the desired compound (23.50 g, 94%) that was carried forward to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481544B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-cdb597b1fba34f34bf560b450d2c9952 |
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| Source note | uspto-grants-2013_07 |
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