HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl bromomalonate → HCID 20144889, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 11446993 | HCID 11446993 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20144889 | HCID 20144889 | — |
Reaction Steps
(ca) 8.05 g of 3,4-dihydro-thieno[2,3-f][1,4]thiazepine-5(2H)-thione were suspended in 40 ml of methylene chloride and treated under argon with a solution of 7.1 ml of diethyl bromomalonate in 40 ml of methylene chloride. After stirring for 2.5 hours, 50 ml of 10 percent potassium hydrogen carbonate solution were added thereto and the mixture was stirred for 30 minutes. The organic phase was separated and the aqueous phase was extracted twice with methylene chloride. After drying with sodium sulfate, the extract was chromatographed on silica gel, whereby diethyl[3,4-dihydrothieno[2,3-f][1,4]thiazepine-8-(5H)-ylidene]malonate was obtained in the form of slightly yellowish crystals of m.p. 87°-89° (cyclohexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735940 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-811cd212c8ff46fb85d5a60900d70316 |
| Source note | uspto-grants-1988_04 |