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Sodium Acetate → Acetic acid-2-allyl-4-benzyloxy-phenyl ester

HRID 278432
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HRID 278432 반응식
[CH2:1]([C:4]1[CH:9]=[C:8]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:7]=[CH:6][C:5]=1[OH:18])[CH:2]=[CH2:3].[CH3:19][C:20]([O-])=[O:21].[Na+]>C(OC(=O)C)(=O)C>[CH2:1]([C:4]1[CH:9]=[C:8]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:7]=[CH:6][C:5]=1[O:18][C:20](=[O:21])[CH3:19])[CH:2]=[CH2:3]
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참가 물질

4

반응물 2

HCID 517045Sodium AcetateHCID 18701949HCID 18701949, 화합물

생성물 1

HCID 22628362Acetic acid-2-allyl-4-benzyloxy-phenyl ester수율 650%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

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온도
80 °C

실험 절차

2-Allyl-4-benzyloxy-phenol (2.87 g, 12 mmol) was taken up in acetic anhydride (40 ml) and NaOAc (150 mg, 1.8 mmol) was added and the mixture heated 18 hr at 80° C. After cooling, the reaction mixture was evaporated to afford an oil which was partitioned between EtOAc and H2O (100 ml) and the aqueous phase was extracted with EtOAc (100 ml) and the combined organic phases were dried with MgSO4, filtered and evaporated to afford acetic acid-2-allyl-4-benzyloxy-phenyl ester as a pale yellow oil (3.30 g, 11.7 mmol, 97%), MS: m/e=282.1 (M+).

후처리

  1. temperatureAfter cooling
  2. customthe reaction mixture was evaporated
  3. customto afford an oil which
  4. customwas partitioned between EtOAc and H2O (100 ml)
  5. extractionthe aqueous phase was extracted with EtOAc (100 ml)
  6. dry with materialthe combined organic phases were dried with MgSO4
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-ccf186c7ffdf4382b87873298c0fa13c
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06359138B1

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