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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035686Generated: October 30, 2026

Sodium hydride → HCID 66740127, compound

https://huagongshe.com/reaction/1035686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-(4-oxocyclohexyl)benzoateHCID 22633634—
ReactantHCID 86662109HCID 86662109—
SolventDimethylformamideHCID 6228—
ProductHCID 66740127HCID 6674012772.1%

Reaction Conditions

Temperature4 °C

Reaction Steps

5.63 g of tert-butyl diethylphosphoacetate (20.3 mmol, 1 eq.) are placed in 20 mL of dimethylformamide with stirring. The solution is cooled to a temperature of 4° C. by placing it in an ice bath, and 0.536 g of sodium hydride (22.33 mmol, 1.1 eq.) is then added portionwise. After 30 minutes, 5 g of ethyl 4-(4-oxo-cyclohexyl)benzoate (20.3 mmol, 1 eq.) are added and the ice bath is removed. After stirring for 1 hour, the flask is placed in an ice bath to cool the reaction medium to a temperature of 4° C., and 0.049 g of sodium hydride (2.04 mmol, 0.1 eq.) is added. The ice bath is removed and, after 30 minutes, the mixture is poured into 200 mL of 1N potassium hydrogen sulfate and extracted with 300 mL of ethyl ether. The organic phase is washed 4 times with brine. The organic phase is dried over sodium sulfate and evaporated. The residue is chromatographed on silica gel, eluting with a gradient of methanol in dichloromethane ranging from 0% to 5%. 5.04 g of ethyl 4-(4-tert-butoxycarbonylmethylenecyclohexyl)benzoate are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546391B2
Source datasetuspto-grants-2013_10
ORD IDord-5683200e5e6f41d3b5fc30a99ca35f00
Source noteuspto-grants-2013_10