Acetyl chloride → 4-(4-Acetoxyphenoxy)benzoic acid

HRID 23373노트

반응식

HRID 23373 반응식
[C:1](Cl)(=[O:3])[CH3:2].[OH:5][C:6]1[CH:21]=[CH:20][C:9]([O:10][C:11]2[CH:19]=[CH:18][C:14]([C:15]([OH:17])=[O:16])=[CH:13][CH:12]=2)=[CH:8][CH:7]=1>C(Cl)Cl>[C:1]([O:5][C:6]1[CH:21]=[CH:20][C:9]([O:10][C:11]2[CH:19]=[CH:18][C:14]([C:15]([OH:17])=[O:16])=[CH:13][CH:12]=2)=[CH:8][CH:7]=1)(=[O:3])[CH3:2]

참가 물질

4

반응물 2

HCID 6367Acetyl chlorideHCID 6155424-(4-Hydroxy-phenoxy)-benzoic acid

생성물 1

HCID 225734654-(4-Acetoxyphenoxy)benzoic acid수율 87%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Acetylchloride (1.5 mL, 21 mmol) is added to a solution of 4-(4-hydroxyphenoxy)benzoic acid (2.3 g, 10 mmol) and TEA (2.9 mL, 21 mmol) in CH2Cl2 (50 mL). The reaction is stirred for 16 hours at room temperature. The reaction mixture is diluted with CH2Cl2 and washed three times with saturated NaHCO3. The organic layer is dried (MgSO4), filtered and concentrated in vacuo. The resulting material is dissolved in dioxane (6 mL). Aqueous LiOH (1N, 930 μL) is added, and the reaction is allowed to stir for one hour at room temperature. The reaction mixture is poured into CH2Cl2 and washed twice with KHSO4. The organic layer is dried (MgSO4), filtered and concentrated in vacuo to give 4-(4-acetoxyphenoxy)benzoic acid (1.5 g, 87%). 1H NMR (300 MHz, DMSO) δ 12.80, 7.96, 7.23-7.13, 7.04, 2.29.

후처리

  1. washwashed three times with saturated NaHCO3
  2. dry with materialThe organic layer is dried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. dissolutionThe resulting material is dissolved in dioxane (6 mL)
  6. additionAqueous LiOH (1N, 930 μL) is added
  7. stirringto stir for one hour at room temperature
  8. additionThe reaction mixture is poured into CH2Cl2
  9. washwashed twice with KHSO4
  10. dry with materialThe organic layer is dried (MgSO4)
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-57713b86a77642e28b6eb5f0508e6d42
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06852716B2

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