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HRID 242577생성일: 2026년 10월 24일

Hydrochloric Acid → 2-(2-Bromo-5-chlorophenyl)-4,4-dimethyl-4,5-dihydrooxazole

https://huagongshe.com/ko/reaction/242577

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물2-Amino-2-methyl-1-propanolHCID 11807—
반응물Sodium HydroxideHCID 14798—
반응물Thionyl ChlorideHCID 24386—
반응물Oxalyl chlorideHCID 65578—
반응물2-Bromo-5-chlorobenzoic acidHCID 89027—
반응물Sodium BicarbonateHCID 516892—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-(2-Bromo-5-chlorophenyl)-4,4-dimethyl-4,5-dihydrooxazoleHCID 2313691462.3%

반응 단계

To a suspension of 2-bromo-5-chlorobenzoic acid (1.5 g, 6.4 mmol) in methylene chloride (15 mL) at room temperature was added oxalyl chloride (969 mg, 666 μL, 7.64 mmol) and 2 drops of dimethylformamide; bubbling commenced and the mixture ultimately became homogenous. The mixture was stirred at roorm temperature for 7 hours and concentrated. The resulting acid chloride residue was dissolved in methylene chloride (15 mL). Triethylamine (325 mg, 450 μL, 3.2 mmol) was added, followed by 2-amino-2-methyl-1-propanol (627 mg, 672 μL, 7.04 mmol) and the reaction was allowed to stir at rt 3 h. The mixture was poured into 1 N hydrochloric acid (50 mL), extracted with methylene chloride (2×75 mL). The combined extracts were washed with saturated aqueous sodium bicarbonate, brine and dried over magnesium sulfate, filtered and concentrated and dried in vacuo. The crude amide residue was dissolved in methylene chloride (15 mL) and thionyl chloride (1.29 g, 794 μL, 10.9 mmol) was added. Stirring at room temperature was carried out for 4 h after which the mixture was poured into saturated sodium bicarbonate (50 mL). The pH was adjusted to 9 by the addition of solid sodium bicarbonate and further basified by the addition of several milliliters of aqueous sodium hydroxide (5 N). The biphasic mixture was extracted with methylene chloride (150+50 mL). The combined extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated to afford the crude residue which was purified by silica gel chromatography (80% hexanes/20% ethyl acetate gradient) to yield 2-(2-bromo-5-chloro-phenyl)-4,4-dimethyl-4,5-dihydro-oxazole (1.15 g, 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653096B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-0cf243a3644b4598bdc7e7b8d6a97a96
출처 메모uspto-grants-2014_02