HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → S-benzylthiobenzimidate hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Thiobenzamide | HCID 683563 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S-benzylthiobenzimidate hydrobromide | HCID 12624654 | 85% |
Reaction Steps
To a solution of thiobenzamide (0.307 g, 2.24 mmol) in CH2Cl2 (11 mL) was added benzyl bromide (0.26 mL, 2.19 mmol) and the resultant solution was heated to reflux for 2 h. The mixture was cooled to room temperature and concentrated under reduced pressure. The resultant yellow solid was dried under vacuum to provide S-benzylthiobenzimidate hydrobromide (0.573 g, 85%). 1H NMR (DMSO-d6) δ4.76 (s, 2H), 7.34-7.44 (m, 3H), 7.51-7.54 (m, 2H), 7.61-7.66 (m, 2H), 7.78-7.83 (m, 1H), 7.88-7.91 (m, 2H), 11.92 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06734191B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-6a77445ff1dc452389811ea7b834a800 |
| Source note | uspto-grants-2004_05 |