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2-Phenylethanol → 2-Phenylethyl Acetate

HRID 1264191
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HRID 1264191 반응식
[C:1]([O:4][C:5](=[O:7])[CH3:6])(=O)[CH3:2].[C:8]1(CCO)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>C(Cl)Cl.O=[V].Cl.Cl.Cl>[CH3:6][C:5]([O:4][CH2:1][CH2:2][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:7]
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참가 물질

5

반응물 2

HCID 60542-PhenylethanolHCID 7918Acetic Anhydride

생성물 1

HCID 76542-Phenylethyl Acetate수율 94%

시약·촉매·용매 2

HCID 24410Vanadium trichloride oxide촉매HCID 6344Dichloromethane용매2회

실험 절차

In a dry 50-mL, two-necked, round-bottomed flask, vanadyl chloride (1.9 mg, 0.01 mmol) in 3 mL of anhydrous CH2Cl2 was placed. To the above solution, acetic anhydride (153.1 mg, 141.5 μL, 1.5 mmol) was slowly added at ambient temperature. After about 10 min, a solution of 2-phenylethanol (122 mg, 119.3 μL, 1.0 mmol) in CH2Cl2 (2 mL) was slowly added to the above brownish solution, and the reaction mixture was stirred for 7.5 hours. After completion of the reaction as monitored by TLC, the reaction mixture was quenched with cold, saturated aqueous NaHCO3 solution (5 mL). The resulting separated organic layer was washed with brine, dried (MgSO4), filtered, and evaporated. The crude product was purified by column chromatography on silica gel to yield 154.2 mg of 2-phenethyl acetate (94%) as colorless oil. The substrate, reaction time, and yield of this test are summarized in Entry 2 of the following Table 1.

후처리

  1. customAfter completion of the reaction
  2. customthe reaction mixture was quenched with cold, saturated aqueous NaHCO3 solution (5 mL)
  3. customThe resulting separated organic layer
  4. washwas washed with brine
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. customevaporated
  8. customThe crude product was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-f6dde3fa0c584ba2bdadd4da169aed6d
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06541659B1

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