m-Chloroperbenzoic acid → Ethyl 2-(4-acetoxy-2-methylphenoxy)acetate

HRID 445857노트

반응식

HRID 445857 반응식
C([C:4]1[CH:16]=[CH:15][C:7]([O:8][CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[C:6]([CH3:17])[CH:5]=1)(=O)C.C1C=C(Cl)C=[C:20]([C:25]([O:27]O)=[O:26])C=1>ClCCl>[C:25]([O:27][C:4]1[CH:16]=[CH:15][C:7]([O:8][CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[C:6]([CH3:17])[CH:5]=1)(=[O:26])[CH3:20]

참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 21986544Ethyl 2-(4-acetyl-2-methylphenoxy)acetate

생성물 1

HCID 21986316Ethyl 2-(4-acetoxy-2-methylphenoxy)acetate수율 72%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of ethyl 2-(4-acetyl-2-methylphenoxy)acetate (683) (8.78 g, 37 mmol), mCPBA (2.eq.), and p-TsOH monohydrate (0.15 eq.) in dichloromethane (160 mL) was heated at 40° C. overnight. The reaction was cooled to room temperature and washed with 1M KI (2×200 mL), 5% NaHSO3 (2×150 mL), and water (200 mL). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by silica gel chromatography (0-100% EtOAc in hexanes) to provide ethyl 2-(4-acetoxy-2-methylphenoxy)acetate (684) (72%).

후처리

  1. washwashed with 1M KI (2×200 mL), 5% NaHSO3 (2×150 mL), and water (200 mL)
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe crude material was purified by silica gel chromatography (0-100% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-f11a86ffbbe04e5f990c3155298a406d
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08476308B2

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