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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867809Generated: October 30, 2026

Hexane → Dimethyl (4-ethoxy-3,3-dimethyl-2-oxobutyl)phosphonate

https://huagongshe.com/reaction/867809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantHCID 14302194HCID 14302194—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl (4-ethoxy-3,3-dimethyl-2-oxobutyl)phosphonateHCID 1430219572.2%

Reaction Steps

To a solution of dimethyl methylphosphonate (7.18 g, 57.5 mmol) in anhydrous THF (100 ml) was added under argon atmosphere a solution of n-butyl lithium in hexane (1.61N, 35.7 ml, 57.5 mmol) at 31 78° C. The reaction mixture was stirred for 30 min. and a solution of ethyl 2,2-dimethyl-4-oxahexanoate (4.00 g, 23.0 mmol) in anhydrous THF (15 ml) was added at -78° C. The resulting mixture was stirred for 30 min., allowed to warm to room temperature and stirred for one hour. The resulting mixture was then neutralized with acetic acid, then water (20 ml) was added, and the mixture was concentrated. Ethyl acetate (120 ml) and water (30 ml) were added to the residue. The organic layer was separated, washed with water (50 ml) and with brine, dried over anhydrous magnesium sulfate, and concentrated. Distillation of the residue (b.p. 106°-110° C./0.4 mmHg) gave dimethyl 3,3-dimethyl- 2-oxo-5-oxaheptylphosphonate (4.19 g, 16.6 mmol, 72.2%) as an oily material. The product was assigned the structure by the following data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775692
Source datasetuspto-grants-1988_10
ORD IDord-44e3b2879d154f39b76d1cd2c7f80295
Source noteuspto-grants-1988_10