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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017201Generated: October 30, 2026

Chlorotrimethylsilane → HCID 18403070, compound

https://huagongshe.com/reaction/1017201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantDibenzyl 2-methylenepentanedioateHCID 10947302—
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 dichloroemthane 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=-butyl, R1=H) (2.9 g, 40%) as a clear and colorless oil. Rf 0.12 (3:1, Hex./EtOAc 5% AcOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479471B1
Source datasetuspto-grants-2002_11
ORD IDord-993a6dabf0aa4743b28ff05eb46ac5bc
Source noteuspto-grants-2002_11