HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Bromomethyl)-3-chloro-2-fluorobenzene → (3-Chloro-2-fluorophenyl)methanethiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Bromomethyl)-3-chloro-2-fluorobenzene | HCID 522827 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3-Chloro-2-fluorophenyl)methanethiol | HCID 2761442 | 89.8% |
Reaction Steps
3-Chloro-2-fluorobenzyl bromide (1.00 g) and thiourea (0.35 g) were heated together at reflux in ethanol (10 ml) for 1 hour. The solvent was removed in-vacuo and the residue was suspended in 10% aqueous sodium hydroxide (10 ml) and heated at reflux for 3 hours. The solution was then acidified with conc. HCl and extracted into ether. Concentration of the organic phase in-vacuo gave the subtitle compound as a pale yellow oil (0.71 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875868B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-eb311a1918584c879ef58af8ea0e1957 |
| Source note | uspto-grants-2005_04 |