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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355197생성일: 2026년 10월 24일

Benzoyl chloride → 2,5-anhydro-6-O-benzoyl-D-mannitol

https://huagongshe.com/ko/reaction/355197

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물TriethylamineHCID 8471—
반응물2,5-anhydro-D-mannitolHCID 73544—
용매TetrahydrofuranHCID 8028—
생성물2,5-anhydro-6-O-benzoyl-D-mannitolHCID 13174975—

반응 단계

7.9 g. (6.5 ml., 56.3 mmol.) of benzoyl chloride and 5.7 g. (8.02 ml., 56.3 mmol.) of triethylamine were added to a suspension of 8.4 g. (51.2 mmol.) of 2,5-anhydro-D-mannitol in 100 ml. of tetrahydrofuran. The reaction mixture was refluxed for 5 hrs., allowed to cool to room temperature and evaporated at room temperature and 200 ml. of chloroform is added to the residue. The solids were removed by filtration and washed with chloroform and the chloroform filtrate and washings were combined and evaporated at reduced pressure. The residue was filtered through 200 ml. of silica gel utilizing chloroform and 5% methanol/chloroform to elute the dibenzoate and 5% methanol/chloroform and 10% methanol/chloroform to elute the monobenzoate. The fractions containing the monobenzoate (as indicated by thin layer chromatography) were combined and evaporated at reduced pressure to an uncrystallizable, very thick oil. The oil was distilled in a Kugelrohr apparatus at 135°-145° C. and 40μ. to obtain a thick, pale yellow oil (2.50 g.) [α]D =+46.191° (methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04378369
출처 데이터셋uspto-grants-1983_03
ORD IDord-64df85ce323a4c5e8f74aa4659206277
출처 메모uspto-grants-1983_03