Acetic Acid → Methyl 3-(4-amino-3-cyclopentoxyphenyl)-E-propenoate hydrochloride

HRID 327601노트

반응식

HRID 327601 반응식
[CH:1]1([O:6][C:7]2[CH:8]=[C:9](/[CH:16]=[CH:17]/[C:18]([O:20][CH3:21])=[O:19])[CH:10]=[CH:11][C:12]=2[N+:13]([O-])=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.C(O)(=O)C.[ClH:26]>CO.C(OCC)C.[Fe]>[ClH:26].[NH2:13][C:12]1[CH:11]=[CH:10][C:9](/[CH:16]=[CH:17]/[C:18]([O:20][CH3:21])=[O:19])=[CH:8][C:7]=1[O:6][CH:1]1[CH2:2][CH2:3][CH2:4][CH2:5]1

참가 물질

7

반응물 3

HCID 176Acetic AcidHCID 313Hydrochloric Acid2회HCID 15052471Methyl 3-(3-cyclopentoxy-4-nitrophenyl)-E-propenoate

생성물 1

HCID 70056690Methyl 3-(4-amino-3-cyclopentoxyphenyl)-E-propenoate hydrochloride

시약·촉매·용매 3

HCID 23925Iron촉매HCID 887Methanol용매HCID 3283Diethyl Ether용매

실험 절차

To a stirred solution of 2.1 g (7.2 mmol) of methyl 3-(3-cyclopentoxy-4-nitrophenyl)-E-propenoate in 30 mL of methanol was added 6.3 mL (110.1 mmol) of glacial acetic acid and 2.0 g (35.8 mmol) of iron filings. The mixture was warmed to reflux and stirred for 16 hours after which time it was cooled to room temperature, filtered over Celite 545, and concentrated. Liquid chromatography over 200 g of silica gel using 50% ethyl acetate in hexane provided a pure oil. The product was dissolved in anhydrous ethyl ether, subjected to a stream of anhydrous hydrogen chloride gas upon which time an analytically pure, hydrochloride solid formed. The desired solid was collected, washed several times with anhydrous ethyl ether, and dried in vacuo.

후처리

  1. temperatureThe mixture was warmed
  2. temperatureto reflux
  3. filtrationfiltered over Celite 545
  4. concentrationconcentrated
  5. customLiquid chromatography over 200 g of silica gel using 50% ethyl acetate in hexane provided a pure oil
  6. customformed
  7. customThe desired solid was collected
  8. washwashed several times with anhydrous ethyl ether
  9. customdried in vacuo

출처 및 근거

ORD 기록
ord-d9348e125ce049f9ad6fb7b970c21b4e
출처 데이터셋
uspto-grants-1993_12
특허 번호
US05274002

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