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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1857320생성일: 2026년 10월 26일

Acetone Cyanohydrin → HCID 178463114, 화합물

https://huagongshe.com/reaction/1857320

반응식

참여 물질

역할이름HCID투입량
반응물Acetone CyanohydrinHCID 6406—
반응물TriethylamineHCID 8471—
반응물3-(4,5-Dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl chlorideHCID 11255083—
반응물HCID 178463041HCID 178463041—
용매ChloroformHCID 6212—
생성물HCID 178463114HCID 17846311467.3%

반응 단계

To 2.75 g of 3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoic acid were added 30 ml of benzene, then 1.7 ml of thionyl chloride and a drop of pyridine to heat at reflux for 3 hours. The reaction solution was cooled down. The solvent was distilled out under reduced pressure to give 2.90 g of 3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl chloride. Separately 0.93 g of 1-ethyl-5-hydroxypyrazole hydrochloride was dissolved in 20 ml of chloroform, and 1.60 g of triethylamine was added, while cooling with ice. Into the obtained solution was added dropwise 10 ml of a chloroform solution containing 1.90 g of 3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl chloride to stir at room temperature for 30 minutes, and 0.76 g of triethylamine and 0.16 g of acetone cyanohydrin were added to further stir overnight. The reaction solution was washed with dilute hydrochloric acid, then with a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was distilled out under reduced pressure. Methanol was added to the residue. The obtained crystals were separated by filtration to give 1.59 g of the title compound as white crystals. m.p. 183~184.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06147031
출처 데이터셋uspto-grants-2000_11
ORD IDord-5dfc44ea4ec545fa92afe03413a59bb1
출처 메모uspto-grants-2000_11