Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913139Generated: November 3, 2026

Water → 2,2,2-Trifluoro-N-(4-hydroxycyclohexyl)-N-methylacetamide

https://huagongshe.com/reaction/1913139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178523812HCID 178523812—
SolventDimethylacetamideHCID 31374—
Product2,2,2-Trifluoro-N-(4-hydroxycyclohexyl)-N-methylacetamideHCID 58468184—

Reaction Conditions

Temperature0 °C

Reaction Steps

5 g of 2,2,2-trifluoro-N-(4-hydroxy-cyclohexyl)-acetamide (148) were dissolved in 25 mL of dimethyl acetamide, 625 mg of 95% sodium hydride were added and the reaction mixture was cooled to 0° C. 1.64 mL of iodomethane were added slowly and the reaction mixture was allowed to warm to room temperature. Upon completion, the reaction mixture was poured into water, extracted three times with methyl tert. butyl ether and the combined organic layer was extracted once with brine, dried over sodium sulfate and evaporated to dryness. The residue was taken up in water and lyophilized to remove remainders of dimethyl acetamide to yield 4.0 g of product. Rt=0.95 min (Method C). Detected mass: 226.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609691B2
Source datasetuspto-grants-2013_12
ORD IDord-b9fbe1f5f0534c0f9f0e859b28aebcff
Source noteuspto-grants-2013_12