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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604751Generated: October 25, 2026

Diphenylphosphine → Nmdpp

https://huagongshe.com/reaction/1604751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylphosphineHCID 70017—
Reactant2-Chloro-4-methyl-1-(1-methylethyl)cyclohexaneHCID 85951—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductNmdppHCID 1266533854.1%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Diphenylphosphine (140 g, 0.75 mol) was charged into a 2-L, 3-neck, round-bottom flask in a glove box under a nitrogen atmosphere. The reactor was connected to a nitrogen manifold. Freshly distilled tetrahydrofuran (400 mL) was added to the mixture and the mixture was cooled to -20° C. Normal butyllithium (1.6 M in hexanes, 468 mL, 0.75 mol) was added over a 2 hour period. The cold bath was removed and the orange solution was warmed to room temperature. After stirring at room temperature for 0.5 hour, (-)-menthyl chloride (129 g, 0.74 mol) was added. The mixture was stirred at room temperature for 21 hours and then heated at reflux for 40 hours. The reaction mixture was cooled to room temperature and quenched with H2O (125 mL). After stirring for 2 hours, the organic layer was separated, washed with H2O (125 mL) and concentrated to an oil. The resulting material was distilled under vacuum until crystal formation was observed in the distillation condenser to give about 130 g of crude NMDPP in the pot.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994587
Source datasetuspto-grants-1999_11
ORD IDord-2f82544475b74aa2b8f9bca6bec8bd1a
Source noteuspto-grants-1999_11