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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275059생성일: 2026년 10월 26일

Triethyl Citrate → 2-(Oxolan-3-yl)ethan-1-ol

https://huagongshe.com/reaction/275059

반응식

참여 물질

역할이름HCID투입량
반응물Triethyl CitrateHCID 6506—
반응물TetrahydrofuranHCID 8028—
반응물HCID 178418361HCID 178418361—
용매EthanolHCID 702—
생성물(Oxan-4-yl)methanolHCID 27735733.6%
생성물2-(Oxolan-3-yl)ethan-1-olHCID 1112622549%

반응 단계

400 ml of triethyl citrate were hydrogenated at 225° C. and 200 bar together with 1100 ml of tetrahydrofuran and 60 g of catalyst H (3-mm tablets) until the take-up of hydrogen had ceased. The reaction product was freed from tetrahydrofuran and ethanol and distilled under reduced pressure, giving 93.6 g (49%) of 3-(2'-hydroxyethyl)tetrahydrofuran and 6.8 g (3.6%) of 4-hydroxymethyltetrahydropyran.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05391771
출처 데이터셋uspto-grants-1995_02
ORD IDord-e0c800179a6a41f3800b0b39c6564e34
출처 메모uspto-grants-1995_02