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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834544Generated: October 30, 2026

Hydrochloric Acid → Diisobutyl-n-heptyl-phosphine oxide

https://huagongshe.com/reaction/1834544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylphosphinyl chlorideHCID 22481195—
ReactantHCID 178443916HCID 178443916—
SolventTetrahydrofuranHCID 8028—
ProductDiisobutyl-n-heptyl-phosphine oxideHCID 22481194—

Reaction Steps

A solution of di-isobutylphosphinyl chloride* (3.9g., 0.02 mole) in tetrahydrofuran (50 ml.) was added dropwise to a refluxing solution of n-heptylmagnesium bromide (prepared from magnesium turnings (1.2g., 0.05 mole), n-heptyl bromide (9.0g., 0.05 mole) and tetrahydrofuran (100 ml.)). The mixture was heated under reflux for 18 hours. After cooling to room temperature, the reaction mixture was poured onto ice and 2N HCl (300 ml.), and extracted with methylene dichloride (4 × 200 ml.). The combined extracts were washed with lithium hypochlorite solution, 2N NaOH solution and finally with water, then dried (MgSO4). The solvent was removed by distillation and the residual yellow oil (8g.) was eluted with chloroform down a silica gel column. The product (Rf = 0.1- 0.2 on silica t.l.c. (CHCl3)) was finally distilled to yield diisobutyl-n-heptyl-phosphine oxide as a colourless liquid, bp. 120°-2°/0.03 mm. (Found C 68.8; H 13.0; C15H33OP requires C 69.3; H, 12.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04070496
Source datasetuspto-grants-1978_01
ORD IDord-e6cf7232ea8649b1a38435e3869382f2
Source noteuspto-grants-1978_01