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Sodium Hydroxide → 3-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenol

HRID 1994075
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반응식

HRID 1994075 반응식
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][O:14][C:15]1[CH:16]=[C:17]([O:21]C(=O)C)[CH:18]=[CH:19][CH:20]=1.[OH-].[Na+]>CO.O>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[N:4][C:3]=1[CH2:13][O:14][C:15]1[CH:16]=[C:17]([OH:21])[CH:18]=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 68677549Acetic acid 3-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl ester

생성물 1

HCID 686778803-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenol

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

To a stirred solution of the title A compound, acetic acid 3-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl ester (3.92 g, 12.14 mmol) in methanol (15 mL) is added sodium hydroxide (0.97 g, 24.27 mmol) in water (15 mL) at RT. The reaction mixture is stirred for 4 h. The reaction mixture is concentrated at reduced pressure, poured into water, the aqueous layer is separated, washed with ethyl acetate twice, acidified with concentrated HCl and extracted three times with ethyl acetate. The combined ethyl acetate extract is dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 3-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-phenol as a white solid.

후처리

  1. concentrationThe reaction mixture is concentrated at reduced pressure
  2. additionpoured into water
  3. customthe aqueous layer is separated
  4. washwashed with ethyl acetate twice
  5. extractionextracted three times with ethyl acetate
  6. extractionThe combined ethyl acetate extract
  7. dry with materialis dried over anhydrous magnesium sulfate
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-9868992d089540128196abbcfb30ac5a
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07652061B2

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