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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377189Generated: October 30, 2026

Chlorotrimethylsilane → HCID 18403070, compound

https://huagongshe.com/reaction/377189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant2,4-Di(benzyloxycarbonyl)butyl(methyl)-O-benzylphosphinic acidHCID 15885218—
ReactantHCID 178454911HCID 178454911—
SolventDichloromethaneHCID 6344—
ProductHCID 18403070HCID 1840307040.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Butylphosphinic acid (2.0 g, 16 mmol) in 80 mL of dry dichloromethane was cooled to 0° C. under an atmosphere of nitrogen. Triethylamine (6.7 g, 66 mmol) was added followed by trimethylsilyl chloride (58 mL, 58 mmol, 1.0 M in dichloromethane). The mixture was stirred at 0° C. for 10 minutes and dibenzyl 2-methylenepentanedioate (2)(6.4 g, 20 mmol) in 20 mL of dichloromethane was added. The cold bath was removed and the reaction warmed to room temperature and stirred overnight. The mixture was then cooled to 0° C. and quenched by the slow addition of 5% hydrochloric acid. The dichloromethane layer was then removed and washed with 5% hydrochloric acid and with brine. The organic layer was dried (MgSO4) and evaporated to give a clear light golden liquid. The liquid was purified by flash chromatography and eluted with 3:1 hexane/ethyl acetate containing 5% acetic acid. The desired fractions were combined and evaporated to give butyl[2,4-di(benzyloxycarbonyl)butyl]phosphinic acid (3,R=n-butyl, R1=H) (2.9 g, 40%) as a clear and colorless oil. Rf0.12 (3:1, Hex./EtOAc 5% AcOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025345
Source datasetuspto-grants-2000_02
ORD IDord-ba9a2206c9474e41be93a2640223114c
Source noteuspto-grants-2000_02