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HRID 392813作成日:2026年10月24日

Triethylamine → HCID 86587276、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
反応物L-Malic AcidHCID 222656—
反応物(S)-2-(2,2-Dimethyl-5-oxo-1,3-dioxolan-4-yl)acetic acidHCID 641720—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物HCID 86587276HCID 8658727699.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06803378B2
出典データセットuspto-grants-2004_10
ORD IDord-cbfcffe2f321494b9f6b949aed7e6a8e
出典メモuspto-grants-2004_10