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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977853Generated: October 30, 2026

Sodium hydride → HCID 19966068, compound

https://huagongshe.com/reaction/977853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantMethylthiomethyl p-tolyl sulfoneHCID 548421—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductHCID 19966068HCID 1996606889%

Reaction Steps

990 mg (22.7 mmol) of sodium hydride (as a 55% w/w suspension in mineral oil) were washed twice with hexane, and suspended in 40 ml of dimethylformamide. 4.35 g (20.1 mmol) of methylthiomethyl p-tolyl sulfone were added to this suspension and, after 5 minutes, 3.1 ml (22.2 mmol) of cyclohexylmethyl bromide were added. The mixture was allowed to return to room temperature, after which it was stirred for 5 hours. At the end of this time, a dilute aqueous solution of ammonium chloride was added to stop the reaction. The reaction mixture was then extracted with diethyl ether, and the extract was washed with a saturated aqueous solution of sodium chloride. The solvent was then removed by distillation under reduced pressure. The resulting residue was subjected to column chromatography through 100 g of silica gel. Elution with a 1:3 by volume mixture of ethyl acetate and hexane afforded 5.57 g (yield 89%) of the title compound as crystals, melting at 65°-66° C. (after recrystallization from a mixture of diisopropyl ether and hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614550
Source datasetuspto-grants-1997_03
ORD IDord-7a57a676e1bc43c9b5b2a8809fed5ce9
Source noteuspto-grants-1997_03