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Lithium Hydroxide → Rac-trans-cyclopentane-1,2-dicarboxylic acid monoethyl ester

HRID 1641793
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HRID 1641793 반응식
[CH2:1]([O:3][C:4]([C@@H:6]1[CH2:10][CH2:9][CH2:8][C@H:7]1[C:11]([O:13]CC)=[O:12])=[O:5])[CH3:2].[OH-].[Li+]>O>[CH2:1]([O:3][C:4]([C@@H:6]1[CH2:10][CH2:9][CH2:8][C@H:7]1[C:11]([OH:13])=[O:12])=[O:5])[CH3:2]
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참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 57377009diethyl (1R,2R)-cyclopentane-1,2-dicarboxylate

생성물 1

HCID 57652016Rac-trans-cyclopentane-1,2-dicarboxylic acid monoethyl ester수율 27.7%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a solution of rac-trans-cyclopentane-1,2-dicarboxylic acid diethyl ester (393 mg, 1.84 mmol) was added a solution of lithium hydroxide (75.5 mg, 1.8 mmol) in water (7 mL). The reaction mixture was stirred at room temperature for 30 minutes and then heated to 55° C. for 1 hr. The reaction mixture was cooled and evaporated under reduced pressure. The residue was dissolved in 25 mL water and washed with diethyl ether (2×5 mL). The pH of the aqueous layer was adjusted to pH 5 with 1N hydrochloric acid and extracted with methylene chloride (2×5 mL) and ethyl acetate (5 mL). The combined organic layers were dried over magnesium sulfate, filtered and evaporated to dryness under vacuum to give rac-trans-cyclopentane-1,2-dicarboxylic acid monoethyl ester (95 mg) that was used without further purification.

후처리

  1. temperatureheated to 55° C. for 1 hr
  2. temperatureThe reaction mixture was cooled
  3. customevaporated under reduced pressure
  4. dissolutionThe residue was dissolved in 25 mL water
  5. washwashed with diethyl ether (2×5 mL)
  6. extractionextracted with methylene chloride (2×5 mL) and ethyl acetate (5 mL)
  7. dry with materialThe combined organic layers were dried over magnesium sulfate
  8. filtrationfiltered
  9. customevaporated to dryness under vacuum

출처 및 근거

ORD 기록
ord-6a1aae0deae940368322abe54778c78f
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08115011B2

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