돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325253생성일: 2026년 10월 26일

Mandelonitrile → Cyano(phenyl)methyl 3,6-dichloro-2-methoxybenzoate

https://huagongshe.com/reaction/325253

반응식

참여 물질

역할이름HCID투입량
반응물MandelonitrileHCID 10758—
반응물3,5-DimethylpyridineHCID 11565—
반응물Benzoyl chloride, 3,6-dichloro-2-methoxy-HCID 82609—
용매DichloromethaneHCID 6344—
생성물Cyano(phenyl)methyl 3,6-dichloro-2-methoxybenzoateHCID 13206467—

반응 조건

온도10 °C

반응 단계

Benzaldehyde cyanohydrin (13.3 grams; 0.100 moles), 3,5-lutidine (11 grams) and methylene chloride (100 ml) were placed in a 500 ml. 3-necked glass reaction flask equipped with a mechanical stirrer, thermometer, condenser and addition funnel. This mixture was cooled to 10° C. by means of an ice bath and 2-methoxy-3,6-dichlorobenzoic acid chloride (23.9 grams; 0.10 moles) was added dropwise with the temperature of the mixture maintained at 5°-10° C. After the addition of the acid chloride was completed, the reaction mixture was stirred for an additional three hours at room temperature. After the reaction was completed, the mixture was washed three times with water, dried over anhydrous magnesium sulfate, filtered and concentrated by distillation. The residue was heated to a temperature of 150° C. under vacuum from a vacuum pump. Then the residue was dissolved in cyclohexane, treated with nuchar, filtered and stripped dry to give an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04440567
출처 데이터셋uspto-grants-1984_04
ORD IDord-9c4209d943364f8ca43ea4ab23b9381f
출처 메모uspto-grants-1984_04