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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392813생성일: 2026년 10월 24일

Triethylamine → HCID 86587276, 화합물

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물L-Malic AcidHCID 222656—
반응물(S)-2-(2,2-Dimethyl-5-oxo-1,3-dioxolan-4-yl)acetic acidHCID 641720—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물HCID 86587276HCID 8658727699.8%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06803378B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-cbfcffe2f321494b9f6b949aed7e6a8e
출처 메모uspto-grants-2004_10