Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910571Generated: October 28, 2026

Ammonium Chloride → Benzyl-di-t-butylphosphine

https://huagongshe.com/reaction/910571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDi-tert-butylchlorophosphineHCID 139566—
ReactantHCID 178418336HCID 178418336—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl-di-t-butylphosphineHCID 11170394—

Reaction Steps

Di-t-butylchlorophosphine (75.0 g (0.415 mole)) and 0.5 mole of 12M solution of benzylmagnesium chloride in THF (200 ml) were refluxed under argon for 2 days. The reaction mixture was allowed to cool off to RT and an aqueous solution of ammonium chloride was added slowly. The organic phase was separated, and dried with magnesium sulfate. After removal of the solvent, the product was purified by distillation in vacuum. The yield of benzyl-di-t-butylphosphine was 94.3 g (96%) with b.p. 56-59° C./0.1 mm. 31-P-NMR (CDCl3)+36.63 ppm. 1H NMR (CDCl3) 1.18 (s, 9H, Me3C), 1.20 (s, 9H, Me3C), 2.90 (d, 2JPH=2.92 Hz, P—CH2-Ph), 7.1-7:6 (m, 5H, aromatic protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022152B2
Source datasetuspto-grants-2011_09
ORD IDord-a042a629317b40d59d55cbe9c9e50021
Source noteuspto-grants-2011_09