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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22503생성일: 2026년 10월 24일

Hydrochloric Acid → 4-(2-Hydroxy-3-phenoxypropoxy)mandelic acid

https://huagongshe.com/ko/reaction/22503

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium HydroxideHCID 14797—
반응물Phenyl glycidyl etherHCID 31217—
반응물2-Hydroxy-2-(4-hydroxyphenyl)acetic acid, sodium salt hydrateHCID 23698133—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-(2-Hydroxy-3-phenoxypropoxy)mandelic acidHCID 1993044753%

반응 단계

7.5 g (50 mmol) of 2,3-epoxypropyl phenyl ether (phenyl glycidyl ether) are added to a suspension of 10.4 g (50 mmol) of 4-hydroxymandelic acid sodium salt monohydrate, and 300 mg (5.0 mmol) of potassium hydroxide in 25 ml of methanol, and the mixture is refluxed for 8 hours. The homogeneous reaction mixture is then diluted with 300 ml of water, acidified with 25 ml of concentrated hydrochloric acid and extracted three times with dichloromethane. The organic phases are washed with water, combined, dried over magnesium sulfate and concentrated on a vacuum rotary evaporator to give 8.4 g (53%) of 4-(2-hydroxy-3-phenoxypropoxy)mandelic acid as a yellowish resin (compound (204), Table 2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428162
출처 데이터셋uspto-grants-1995_06
ORD IDord-0238d4fb94e6474d902609c0913f4dc0
출처 메모uspto-grants-1995_06