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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2226276생성일: 2026년 10월 26일

Hydrochloric Acid → Methyl 7-phenyl-3,5-dihydroxy-6-heptenoate

https://huagongshe.com/reaction/2226276

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Methyl 7-phenyl-5-hydroxy-3-oxo-6-heptenoateHCID 53740643—
촉매Chlorotitanium triisopropoxideHCID 3084342—
용매MethanolHCID 887—
생성물Methyl 7-phenyl-3,5-dihydroxy-6-heptenoateHCID 5438493465.2%

반응 조건

온도-10 °C

반응 단계

700 mg of methyl 7-phenyl-5-hydroxy-3-oxo-6-heptenoate (2.82 mmol) are dissolved in 25 cm3 of methanol and then cooled to -10° C. 0.71 cm3 of titanium chloride triisopropoxide (2.82 mmol) is added. The mixture is stirred for 20 minutes at -10° C. 207.8 mg of sodium cyanoborohydride (3.1 mmol) are then added and the mixture is then stirred for 3 hours 45 minutes at a temperature between -5° and 0° C. 5 cm3 of water and 1 cm3 of concentrated hydrochloric acid are added. After evaporation of the methanol under reduced pressure, the mixture is taken up in 50 cm3 of dichloromethane. The organic phase is washed with 25 cm3 of a saturated sodium bicarbonate solution and then with 25 cm3 of water and is then dried over sodium sulphate. After filtration and concentration to dryness, the residue obtained is treated with methanol. There is thus obtained, with a yield of 55%, 460 mg of methyl 7-phenyl-3,5-dihydroxy-6-heptenoate for which the syn/anti ratio is equal to 80/20.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05347039
출처 데이터셋uspto-grants-1994_09
ORD IDord-023e42b75a2240e9b7673525036c317b
출처 메모uspto-grants-1994_09