Acetic Acid → 4-METHOXYISOBENZOFURAN-1(3H)-ONE

HRID 465956노트

반응식

HRID 465956 반응식
[OH:1][C:2]1([C:11]([OH:13])=[O:12])[CH:10]=[CH:9][CH:8]=[CH:7][CH:3]1[C:4]([OH:6])=[O:5].[C:14](O)(=[O:16])C.[BH4-].[Na+].Cl>O1CCCC1>[CH3:14][O:1][C:2]1([C:11]([OH:13])=[O:12])[CH:10]=[CH:9][CH:8]=[CH:7][CH:3]1[C:4]([OH:6])=[O:5].[CH3:14][O:16][C:10]1[CH:9]=[CH:8][CH:7]=[C:3]2[C:2]=1[CH2:11][O:13][C:4]2=[O:6]

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 4311764Sodium borohydrideHCID 22292283o-Hydroxyphthalsaure

생성물 2

HCID 111163794-METHOXYISOBENZOFURAN-1(3H)-ONEHCID 19598034o-Methoxyphthalsaure

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Anhydrous 2-methoxyphthalic acid (640 mg), which was prepared with using anhydrous 2-hydroxyphthalic acid by the same procedure as reference example 12, was suspended in tetrahydrofuran (20 ml). Acetic acid (430 mg) and sodium borohydride (135 mg) were added to the suspension. The mixture was stirred for 30 min. at room temperature and for 2 hr. at 50° C. The reaction solution was cooled. 1N hydrochloric acid (7 ml) was added to the cooled solution. The solution was stirred for 15 min. The reaction solution was evaporated. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1→1:1) to give the title compound (314 mg) having the following physical data.

후처리

  1. customat 50° C
  2. temperatureThe reaction solution was cooled
  3. stirringThe solution was stirred for 15 min
  4. customThe reaction solution was evaporated
  5. customThe residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1→1:1)

출처 및 근거

ORD 기록
ord-75a7fb7921aa4b08bcd29bd4f93f2375
출처 데이터셋
uspto-grants-1992_10
특허 번호
US05155104

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