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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358244Generated: October 25, 2026

Sodium hydride → HCID 178420294, compound

https://huagongshe.com/reaction/1358244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Chloro-5,6,7,8-tetrahydroquinazolineHCID 12582969—
ReactantHCID 178521547HCID 178521547—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178420294HCID 178420294—

Reaction Conditions

Temperature50 °C

Reaction Steps

0.5 g (16.7 mmol) of 80% NaH was added in portions to a solution of 1.85 g (105 mmol) of cis-4-phenylcyclohexanol in 30 ml of absolute THF. After this, the mixture was heated for 1 hour at 50° C., and 1.5 g (8.75 mmol) of 4-chloro-5,6,7,8-tetrahydroquinazoline, dissolved in 15 ml of absolute THF, were added dropwise. The reaction mixture was subsequently refluxed for 2 hours. After the mixture has cooled to room temperature, it was poured into saturated NH4Cl solution and this was extracted with ether, and the combined organic phase was dried over MgSO4. The solvent was evaporated in vacuo, and the residue (2.7 g) was purified by flash chromatography over silica gel, using n-hexane/ethyl acetate (2:1). Concentration gave 1.5 g (50.2% of theory), colorless crystals, m.p. 109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596727B1
Source datasetuspto-grants-2003_07
ORD IDord-0cb599674742428c9c869622561ad0b1
Source noteuspto-grants-2003_07