HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromo-2-propanol → 1,3-Bis(benzylthio)-2-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromo-2-propanol | HCID 7287 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Bis(benzylthio)-2-propanol | HCID 15889641 | — |
Reaction Steps
1,3-dibromo-2-propanol (2.18 g.) is added to a stirred suspension of the salt obtained by mixing 2.7 g. benzyl mercaptan and sodium hydride (56% dispersion in mineral oil; 900 mg.) in 50 ml. dry tetrahydrofuran. After 2 hours at room temperature, the solvent is removed and 20 ml. of water is added to the residue. The resultant aqueous mixture is extracted with ether and the extracts washed with water, dried over magnesium sulfate and evaporated to yield 1,3-bis(benzylthio)-2-propanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04036970 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-536ea60cb1c54306a8415c4d5b8a0e4e |
| Source note | uspto-grants-1977_07 |