HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → HCID 21438990, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Reactant | HCID 53693398 | HCID 53693398 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21438990 | HCID 21438990 | 40.6% |
Reaction Steps
A suspension of 38.3 g of cyclohexyl N-carbethoxy-thiocarbamate and 11.56 g of potassium ethylate in 400 ml of methanol was stirred for 2 hours and 12.45 g of chloroacetonitrile were added thereto. The mixture was stirred for 48 hours at room temperature and was then concentrated to dryness. The residue was added to water and the aqueous phase was acidified with hydrochloric acid. The aqueous phase was extracted with ether and the ether phase was dried and concentrated to dryness to obtain 15 g of 2-cyclohexyloxy-4-hydroxy-5-cyanothiazole in the form of white crystals melting at 138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04020076 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-41e5b5170ad14c9e836b0918f2446005 |
| Source note | uspto-grants-1977_04 |