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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600600Generated: October 31, 2026

Chlorotrimethylsilane → HCID 18403062, compound

https://huagongshe.com/reaction/1600600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant2,4-Di(benzyloxycarbonyl)butyl(methyl)-O-benzylphosphinic acidHCID 15885218—
ReactantHCID 178527042HCID 178527042—
SolventDichloromethaneHCID 6344—
ProductHCID 18403062HCID 1840306230.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzylphosphinic acid (2.3 g, 15 mmol) in 150 mL of dry dichloromethane was cooled to 0° C. under a nitrogen atmosphere. Triethylamine (6.5 g, 65 mmol) was added followed by trimethylsilyl chloride (5.8 g, 54 mmol) while the reaction temperature was maintained at 0° C. After 30 minutes dibenzyl 2-methylene-pentanedioate (2) (4.4 g, 13.6 mmol) in 20 mL of dichloromethane was added over 5 minutes. The reaction mixture was allowed to warm to room temperature and stirred overnight. The clear solution was cooled to 0° C. and quenched with 5% hydrochloric acid followed by removal of the organic layer. The organic layer was washed with 5% hydrochloric acid and with brine, dried (MgSO4) and evaporated to give a clear yellow liquid. Purification by flash chromatography and elution with 1:1 hexane/ethyl acetate containing 10% acetic acid yielded 2.0 g (28%) of benzyl[2,4-di(benzyloxycarbonyl)butyl]-phosphinic acid (3, R=CH2Ph, R1 =H) as a clear light yellow oil. Rf 0.37 (1:1 Hexane/EtOAc, 10% AcOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977090
Source datasetuspto-grants-1999_11
ORD IDord-ba0ecbfd4acd430e967a4c7df82621f4
Source noteuspto-grants-1999_11