HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Methoxide → (3-Bromo-5-iodophenyl)-thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-Benzoyl-3-(3-bromo-5-iodophenyl)-thiourea | HCID 57813652 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Bromo-5-iodophenyl)-thiourea | HCID 57813682 | 89.5% |
Reaction Steps
A stirred suspension of 1-Benzoyl-3-(3-bromo-5-iodophenyl)-thiourea (20.70 g, 0.0449 mol) in methanol (303 ml) was treated with sodium methoxide (2.42 g, 0.0449 mol) and stirred at ambient temperature for 4 h. The resultant suspension was evaporated to dryness at reduced pressure. The residue was mixed with water (500 ml) and extracted with ethyl acetate (3×200 ml) which was dried (MgSO4) and the solvent removed in vacuo to give a residue which was triturated with 40-60° petroleum ether/diethyl ether (1:1) to afford (3-Bromo-5-iodophenyl)-thiourea as an off-white solid (14.35 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977340B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-ec356922f60f4dc7b0572fa8765eaeee |
| Source note | uspto-grants-2011_07 |