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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352449Generated: October 29, 2026

Ethyl formate → HCID 70373861, compound

https://huagongshe.com/reaction/2352449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 14304257HCID 14304257—
SolventDiethyl EtherHCID 3283—
ProductHCID 70373861HCID 7037386163.4%

Reaction Steps

34.7 g (0.469 mole) of ethyl formate are added dropwise with stirring to 129.4 g (0.469 mole) of 3,3-dimethyl-4-(4-trifluoromethylthiophenyl)-butan-2-one and 25.3 g (0.469 mole) of sodium methylate in 1 liter of diethyl ether at room temperature, and the mixture is stirred at room temperature for 4 hours after the addition is complete. For work-up, the mixture is extracted with 1 liter of water, and the combined aqueous extracts are washed once with diethyl ether, acidified to pH 1-2 with dilute aqueous hydrochloric acid and extracted with dichloromethane. The dichloromethane phase is dried over sodium sulphate and concentrated in vacuo. 90.5 g of 4,4-dimethyl-5-(4-trifluoromethylthiophenyl)-penten-1-ol-3-one are obtained; these are dissolved in 200 ml of methanol and 17.0 g (0.315 mol) of sodium methylate are added. Concentrating the solution in vacuo gives 97.1 g (75% of theory) of the sodium salt of 4,4-dimethyl-5-(4-trifluoromethylthiophenyl)-1 -penten-1-ol-3-one as a resin, which is further reacted without purification. ##STR875##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877446
Source datasetuspto-grants-1989_10
ORD IDord-48e681581f024d59b485cfa2fec1179e
Source noteuspto-grants-1989_10