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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836450Generated: October 27, 2026

Triethylamine → (S)-(+)-2,2-Dimethyl-5-oxo-1,3-dioxolane-4-acetic Acid, Tert-butyldiphenylsilyl Ester

https://huagongshe.com/reaction/1836450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(S)-2-(2,2-Dimethyl-5-oxo-1,3-dioxolan-4-yl)acetic acidHCID 641720—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product(S)-(+)-2,2-Dimethyl-5-oxo-1,3-dioxolane-4-acetic Acid, Tert-butyldiphenylsilyl EsterHCID 8658727699.8%

Reaction Steps

A solution of (S)-(+)-2,2-dimethyl-5-oxo-1,3-dioxolane-4-acetic acid (2.08 g, 11.9 mmol) in dry dichloromethane (20 ml) was treated with triethylamine (1.83 ml, 13.1 mmol) followed by a solution of t-butylchlorodiphenylsilane (3.44 g, 12.5 mmol) in dichloromethane (5 ml) added dropwise over 5 minutes. After 3 hours at 22° C., the reaction mixture was diluted with toluene (250 ml) washed with water, saturated sodium bicarbonate, brine and dried over magnesium sulfate. Evaporation of the solvent under reduced pressure and chromatography of the residue on silica gel (4×12 cm) using a mixture of toluene and ethyl acetate (0-2%) as eluent gave 4.90 g (99% yield) of the title material as a clear oil. 1H NMR (400 MHz, CDCl3) δ: 1.13 (s, 9), 1.58 (s, 3), 3.05 (m, 2), 4.79 (dd, 1, J=4, 7), 7.4-7.8 (m, 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777440B2
Source datasetuspto-grants-2004_08
ORD IDord-02d156263bf64a58be1f4fb927bd3937
Source noteuspto-grants-2004_08