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Lithium Hydroxide → 4-((1R,2R)-2-hydroxycyclopentyloxy)-3-methoxybenzoic acid

HRID 1908093
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반응식

HRID 1908093 반응식
[OH:1][C@@H:2]1[CH2:6][CH2:5][CH2:4][C@H:3]1[O:7][C:8]1[CH:17]=[CH:16][C:11]([C:12]([O:14]C)=[O:13])=[CH:10][C:9]=1[O:18][CH3:19].[Li+].[OH-]>O1CCOCC1.C(OCC)(=O)C>[OH:1][C@@H:2]1[CH2:6][CH2:5][CH2:4][C@H:3]1[O:7][C:8]1[CH:17]=[CH:16][C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]=1[O:18][CH3:19]
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참가 물질

5

반응물 2

HCID 3939Lithium HydroxideHCID 58550939methyl 4-((1R,2R)-2-hydroxycyclopentyloxy)-3-methoxybenzoate

생성물 1

HCID 585510384-((1R,2R)-2-hydroxycyclopentyloxy)-3-methoxybenzoic acid

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane용매

실험 절차

A solution of methyl 4-[(1R,2R)-2-hydroxycyclopentoxy]-3-methoxy-benzoate (2.8 g, 11 mmol) and LiOH (21 mL of 2.0 M, 42 mmol) in dioxane (20 mL) was stirred at 50° C. overnight. The mixture was diluted with ethyl acetate and was washed with water. The aqueous layer was acidified with 1N HCl and the product was extracted into ethyl acetate. The organics were dried over sodium sulfate, filtered and evaporated to give 4-((1R,2R)-2-hydroxycyclopentyloxy)-3-methoxybenzoic acid. ESI-MS m/z calc. 252.1. found 253.5 (M+1)+; Retention time: 1.07 minutes (3 min run).

후처리

  1. washwas washed with water
  2. extractionthe product was extracted into ethyl acetate
  3. dry with materialThe organics were dried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated

출처 및 근거

ORD 기록
ord-05360cf2fb764c84b4bfd6c92191d9d9
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598164B2

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