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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1408생성일: 2026년 10월 23일

Acetic Anhydride → Lactic Acid

https://huagongshe.com/ko/reaction/1408

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물2-Hydroxyhexanoic acidHCID 99824—
반응물L-Lactic AcidHCID 107689—
용매WaterHCID 962—
생성물Lactic AcidHCID 612—
생성물2-Hydroxyhexanoic acidHCID 99824—

반응 조건

온도140 °C

반응 단계

DL-2-Hydroxycaproic acid (1.00 g, 0.0076 moles), and L-lactic acid (4.5 g of a nominally 85% solution in water; 0.043 moles) were placed in a reaction flask equipped with a distillation head and mechanical stirrer. The flask was heated at 110° C. for 6 hours under low vacuum (aspirator) while water was removed. The temperature was then raised to 140° C. for 6 hours. Acetic anhydride (5.16 g; 0.0506 moles) was added to the oligomer, followed by heating at 80° C. for 14 hours. Excess acetic anhydride and acetic acid were distilled off under low vacuum. Tetrahydrofuran/water (15 mL of 85/15; v/v) was added with stirring and heating at 60° C. for 0.5 hours. The bulk of the solvent was removed by vacuum distillation on a rotary evaporator. The resulting crude product was dissolved in chloroform (20 mL). The chloroform solution was washed twice with millipore water (5 mL) and then dried with MgSO4. The mixture was filtered through a "d" fritted glass funnel and the solvent distilled from the oligomer by rotary evaporation. Final traces of solvents were removed under high vacuum (0.4 mmHg) on a Kugelrohr apparatus at 120° C. to provide acetyl-oligo(D,L-2-hydroxycaproic-co-L-Lactic acid) with n=7.5 for lactic acid and 1.4 for hydroxycaproic acid, MN =763, and MW =1044.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05725841
출처 데이터셋uspto-grants-1998_03
ORD IDord-82348284bdb74ce681d8c47598cef413
출처 메모uspto-grants-1998_03