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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65307생성일: 2026년 10월 23일

Hydrochloric Acid → 1-(3,4-Dimethoxyphenyl)-2-carboxy-6-cyano-6-(i-propyl)-6-(3,4-dimethoxyphenyl)hexane

https://huagongshe.com/ko/reaction/65307

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylamineHCID 7912—
반응물HexaneHCID 8058—
반응물3-(3,4-Dimethoxyphenyl)propionic acidHCID 75019—
반응물5-Chloro-2-(3,4-dimethoxyphenyl)-2-isopropylvaleronitrileHCID 619953—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexamethylphosphoramideHCID 12679—
생성물1-(3,4-Dimethoxyphenyl)-2-carboxy-6-cyano-6-(i-propyl)-6-(3,4-dimethoxyphenyl)hexaneHCID 1402716591.7%

반응 단계

A 1.6M solution of n-butyllithium in hexane (91.8 mL, 147 mmol) was added to a -20° C. solution of diisopropylamine (21 mL, 150 mmol) in THF (480 mL). Hexamethylphosphoramide (56 mL) was added and the mixture maintained at -20° C. while a solution of 3-(3,4-dimethoxyphenyl)propionic acid (15.1 g, 72 mmol) in THF (75 mL) was added. The resulting solution was stirred at room temperature for one hour, and then cooled to -50° C. A solution of 2-(3,4-dimethoxyphenyl)-2-isopropyl-2-(3-iodopropyl)acetonitrile (22, 27.9 g, 72 mmol) was added, and the mixture allowed to warm to room temperature while stirring for 12 hours. The resulting mixture was added to water, acidified with HCl, and extracted three times with ether. The organic layer was washed with aqueous Na2SO3 and brine, dried over Na2SO4, and evaporated to yield 1-(3,4-dimethoxyphenyl)-2-carboxy-6-cyano-6-(i-propyl)-6-(3,4-dimethoxyphenyl)hexane (23, 31 g) as a thick oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04613606
출처 데이터셋uspto-grants-1986_09
ORD IDord-f6b0a2b1d9cd4045ad331bd44de0eb99
출처 메모uspto-grants-1986_09