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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762295Generated: October 30, 2026

Sodium hydride → HCID 20043203, compound

https://huagongshe.com/reaction/1762295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-AdamantanolHCID 64152—
Reactant3-tert-Butyl-2-chloro-1,3,2-oxazaphospholidineHCID 14228109—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20043203HCID 2004320333.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

A 500 ml, three neck flask equipped with a thermometer, an additional funnel and a condenser topped with a nitrogen sweep is charged with 2.62 g (0.06 mol) of sodium hydride. The sodium hydride is washed with two 20 ml portions of hexane and finally suspended in 30 ml of tetrahydrofuran. To the resultant suspension is added dropwise a solution of 9.12 g (0.06 mol) of 1-adamantanol in 75 ml of THF at such rate to keep the reaction temperature between 20°-30° C. The resulting yellow solution is warmed to approximately 40° C. for 1 hour and then cooled in an ice bath. A solution of 10.9 g (0.06 mol) of 3-tert-butyl-2-chloro-1,3,2-oxazaphospholidine in 75 ml of THF is added and stirring continued for 16 hours at room temperature. The resulting cloudy mixture is filtered and the solvent evaporated under reduced pressure. The residue is treated with 200 ml of toluene and the resultant suspension is filtered. The filtrate is concentrated in vacuo to yield a thick syrup. Triturating with methanol gives 6.0 g (33.6%) of a white solid: m.p. 48°-50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831178
Source datasetuspto-grants-1989_05
ORD IDord-9f0c745c2d114de9b458d99e15a2391c
Source noteuspto-grants-1989_05