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Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → Ethyl 3-(4-hydroxyphenyl)butanoate

HRID 2101806
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HRID 2101806 반응식
O1CCCCC1[O:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]([CH3:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:10][CH:9]=1.CC1C=CC(S([O-])(=O)=O)=CC=1.C1C=C[NH+]=CC=1>CCO>[OH:7][C:8]1[CH:9]=[CH:10][C:11]([CH:14]([CH3:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:12][CH:13]=1
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참가 물질

4

반응물 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 57672398Ethyl 3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)butanoate

생성물 1

HCID 51349438Ethyl 3-(4-hydroxyphenyl)butanoate수율 84.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a stirred solution of 38.1 (5.00 g, 17.1 mmol) in EtOH (100 mL) at room temperature was added PPTS. The resulting solution was stirred for 16 hours and then concentrated in vacuo. The residue was purified by flash chromatography (SiO2 gel 60, eluted with 0%-20% EtOAc in hexanes). Fractions containing the desired product were combined and concentrated to give 38.2 (3.00 g, 84%) as a colorless oil. MS ESI (pos.) m/e: 226.1 (M+H2O)+.

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후처리

  1. concentrationconcentrated in vacuo
  2. customThe residue was purified by flash chromatography (SiO2 gel 60, eluted with 0%-20% EtOAc in hexanes)
  3. additionFractions containing the desired product
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-bd34c74cfe7040ccb2ac11d559c4b163
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07572934B2

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