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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392813Generated: October 24, 2026

Triethylamine → HCID 86587276, compound

https://huagongshe.com/en/reaction/392813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantL-Malic AcidHCID 222656—
Reactant(S)-2-(2,2-Dimethyl-5-oxo-1,3-dioxolan-4-yl)acetic acidHCID 641720—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 86587276HCID 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), which was derived from L-malic acid by means known in the art, 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%) 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 numberUS06803378B2
Source datasetuspto-grants-2004_10
ORD IDord-cbfcffe2f321494b9f6b949aed7e6a8e
Source noteuspto-grants-2004_10