HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → 3-Chloro-2-methylbenzofuran-5-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2-Methylbenzofuran-5-carbonitrile | HCID 13663038 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Chloro-2-methylbenzofuran-5-carbonitrile | HCID 13663039 | 24.3% |
Reaction Steps
A solution of 2-methylbenzofuran-5-carbonitrile (J. Het. Chem., 4, 441, 1967) (1.52 g) and sulphuryl chloride (1.49 g) in chloroform (25 ml) was heated under reflux for 9 hours and then cooled. The solution was washed successively with water, dilute sodium hydroxide solution, water and then dried (Na2SO4). Evaporation of the solvent gave a solid which was crystallised twice from methanol to give 3-chloro-2-methylbenzofuran-5-carbonitrile (0.45 g), m.p. 131.5°-133.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496572 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-c514d03169b34892ac5fefc7cdfcf802 |
| Source note | uspto-grants-1985_01 |