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Formic Acid → 5-Formylamino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran

HRID 964795
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HRID 964795 반응식
[NH2:1][C:2]1[C:3]([CH3:15])=[C:4]([CH3:14])[C:5]2[O:9][C:8]([CH3:11])([CH3:10])[CH2:7][C:6]=2[C:12]=1[CH3:13].[CH:16](O)=[O:17]>>[CH:16]([NH:1][C:2]1[C:3]([CH3:15])=[C:4]([CH3:14])[C:5]2[O:9][C:8]([CH3:10])([CH3:11])[CH2:7][C:6]=2[C:12]=1[CH3:13])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 284Formic AcidHCID 100358625-Amino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran

생성물 1

HCID 107521185-Formylamino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran수율 93.3%

실험 절차

5-Amino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran (1.00 g, 4.87 mmol) was dissolved in formic acid (20 ml) and the solution was heated under reflux for 48 hours. The reaction mixture was concentrated under reduced pressure. Saturated sodium bicarbonate solution was added to the residue and the mixture was extracted with chloroform. The extract was washed with saturated saline, dried and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (chloroform-methanol, 97:3) to obtain the desired compound (1.06 g, yield: 93.3%). A part of it was recrystallized from dichloromethan-isopropyl ether to obtain white prisms, m.p. 177°-179° C.

후처리

temperature
the solution was heated
  • temperatureunder reflux for 48 hours
  • concentrationThe reaction mixture was concentrated under reduced pressure
  • additionSaturated sodium bicarbonate solution was added to the residue
  • extractionthe mixture was extracted with chloroform
  • washThe extract was washed with saturated saline
  • customdried
  • concentrationconcentrated under reduced pressure
  • customThe residue was purified by column chromatography on silica gel (chloroform-methanol, 97:3)
  • 출처 및 근거

    ORD 기록
    ord-826c9473c0a548b599cd876365b2e2d4
    출처 데이터셋
    uspto-grants-1998_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05770772

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