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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355101생성일: 2026년 10월 26일

Acetic Acid → 2-Acetoxypropionic Acid

https://huagongshe.com/reaction/355101

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Vinyl AcetateHCID 7904—
반응물TriphenylphosphineHCID 11776—
생성물2-Acetoxypropionic AcidHCID 79041—

반응 조건

온도150 °C

반응 단계

A 300 ml autoclave is charged with 0.110 g of [(C3H5)PdCl]2 (0.6 mmole Pd), 3.15 g. of Ph3P (12 mmole), 83 ml of acetic acid as solvent, and 37 ml of vinyl acetate (0.4 mole). The autoclave was flushed with nitrogen, pressured to 30 psig with carbon monoxide, and heated to 150° C. After reaching 150° C. one milliliter of water was pumped into the reaction solution from a Jurgenson Gauge and the pressure was raised to 700 psig with carbon monoxide. The reaction began absorbing gas as evidenced by a drop in the autoclave pressure. Therefore the autoclave pressure was maintained at 700 psig by feeding carbon monxide from a high-pressure reservoir. In addition, the water concentration in the reaction solution was maintained by addition of one milliliter of water from the Jurgenson Gauge for every 130 psig pressure drop in the high-pressure reservoir. After the addition of a total of five milliliters of water the reaction had consumed 675 psig of carbon monoxide from the high pressure reservoir. At this time the reaction was terminated. The production of α-acetoxypropionic acid was shown by a nuclear magnetic resonance and gas chromatography of the concentrated reaction solution. Pure α-acetoxypropionic acid was isolated from a subsequent fractional distillation. The mass spectrum of other fractions showed ethylidene diacetate (major), propionic acid (minor), and acrylic acid (minor) to be by-products.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04377708
출처 데이터셋uspto-grants-1983_03
ORD IDord-824278905d824834951cae001c4f469d
출처 메모uspto-grants-1983_03