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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500070Generated: October 23, 2026

Dimethylformamide → HCID 86629083, compound

https://huagongshe.com/en/reaction/500070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystButyltriphenylphosphonium bromideHCID 159628—
ProductHCID 86629083HCID 86629083—

Reaction Steps

To a mixture of potassium t-butoxide (2.05 g) and anhydrous N,N-dimethylformamide (60 ml) was added butyltriphenylphosphonium bromide (7.30 g) at room temperature. The mixture was stirred for 15 minutes and then a solution of t-butyl 4-oxocyclohexylcarbamate (1.30 g) in N,N-dimethylformamide (10 ml) was added to the mixture. The reaction mixture was stirred at room temperature overnight and then saturated aqueous ammonium chloride was added to the mixture. The mixture was extracted with toluene, and the organic layer was washed with brine, dried over sodium sulfate, and then the solvent was removed in vacuo. After diethyl ether was added to the residue, the precipitate was filtered off and then the filtrate was concentrated under reduced pressure. The residue was purified by a silica gel chromatography (eluent: gradient from 100% hexane/0% ethyl acetate to 0% hexane/100% ethyl acetate) to give 1.40 g of t-butyl (4-butylidenecyclohexyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767854B2
Source datasetuspto-grants-2010_08
ORD IDord-1fa0f1a583cb4d2886f66a95cb1ac0bd
Source noteuspto-grants-2010_08