HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone Cyanohydrin → HCID 20062230, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiane-3,5-dione | HCID 325286 | — |
| Reactant | HCID 20062229 | HCID 20062229 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20062230 | HCID 20062230 | — |
Reaction Steps
A mixture of 2,2-dimethyl-5-(4-chloro-2-nitrobenzoyloxy)-3,6-dihydro-2H-thiopyran-3-one (8.3 g, 24.3 mmol), triethylamine (6.8 ml, 48.7 mmol) and acetone cyanohydrin (0.5 ml) in 35 ml of acetonitrile is stirred at RT for 16 hours. The reaction mixture is concentrated and taken up in ether. The ether extracts are washed with dilute HCl and with brine, dried and evaporated to dryness. The crude product is purified to give 2-2-dimethyl.4.(4.chloro.2.nitrobenzoyl).2H-thiopyran-3,5-(4H,6H)-dione (compound 1, Table A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05006150 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-b93720fd134c41ebb8e42c9d02b653f1 |
| Source note | uspto-grants-1991_04 |