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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724106Generated: October 27, 2026

tert-BUTYL CHLORIDE → 1-Adamantyl tert-butyl phosphine

https://huagongshe.com/reaction/1724106

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-BUTYL CHLORIDEHCID 10486—
Reactant1-AdamantylphosphineHCID 11768954—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Adamantyl tert-butyl phosphineHCID 68407015—

Reaction Steps

nBuLi (20 cm3, 32 mmol 1.6M soln) was added over 1 hour to a cooled solution of 1-adamantyl phosphine (5.0 g, 30 mmol) in THF (100 cm3). The solution was allowed to warm to room temperature and stirred for a further 2 hours. The solution was recooled to 0° C. and tert-butylchloride (2.78 g, 30 mmol) was added and stirring continued for a further 16 hours at room temperature. The reaction mixture was quenched with water and the aqueous phase extracted with dichloromethane (2×50 ml). The organic phase was dried over sodium sulphate and evaporated in-vacuo to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485739B2
Source datasetuspto-grants-2009_02
ORD IDord-dd3afb9a22d44d6a9990e8eb325cf9de
Source noteuspto-grants-2009_02