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Thionyl Chloride → 5-Oxotetrahydro-2-furancarbonyl chloride

HRID 1419031
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HRID 1419031 반응식
[O:1]=[C:2]1[O:6][CH:5]([C:7]([OH:9])=O)[CH2:4][CH2:3]1.S(Cl)([Cl:12])=O>>[O:1]=[C:2]1[O:6][CH:5]([C:7]([Cl:12])=[O:9])[CH2:4][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 2515245-Oxo-2-tetrahydrofurancarboxylic acid

생성물 1

HCID 108445405-Oxotetrahydro-2-furancarbonyl chloride

실험 절차

A mixture of 4.9 g of 5-oxotetrahydrofuran-2-carboxylic acid and 5.5 ml of thionyl chloride was subjected to reflux for 2 hours. Thionyl chloride was then distilled off under reduced pressure to leave 5-oxotetrahydrofuran-2-carbonyl chloride. This product was mixed with 5.0 g of 2-aminobenzophenone, 200 ml of ethyl acetate and 200 ml of a saturated aqueous solution of sodium hydrogencarbonate, which was stirred for one hour at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-(5-oxotetrahydrofuran-2-carbonyl)aminobenzophenone (6.5 g) as needles, m.p. 100° C.-102° C.

후처리

  1. temperatureto reflux for 2 hours
  • distillationThionyl chloride was then distilled off under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-c8132c9b08414716aa0545424e03200d
    출처 데이터셋
    uspto-grants-1999_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05885979

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