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Sodium Hydroxide → (+-)-trans4-Methylene-2-phenylcyclopentanoic acid

HRID 278275
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HRID 278275 반응식
[CH2:1]=[C:2]1[CH2:6][C@@H:5]([C:7]([O:9]C)=[O:8])[C@H:4]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:3]1.[OH-].[Na+]>CO>[CH2:1]=[C:2]1[CH2:6][C@@H:5]([C:7]([OH:9])=[O:8])[C@H:4]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:3]1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 12537224Methyl 4-methylene-2-phenylcyclopentanecarboxylate, trans-

생성물 1

HCID 18686197(+-)-trans4-Methylene-2-phenylcyclopentanoic acid

시약·촉매·용매 1

HCID 887Methanol용매

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온도
65 °C

실험 절차

To a solution of methyl (+−)-trans4-methylene-2-phenylcyclopentanoate prepared as in Example 1, Step A (28.4 g, 131 mmol) in methanol (400 mL) was added 5N sodium hydroxide (131 mL, 656 mmol). The reaction was heated at 65° C. for 1 h then cooled and concentrated. The residue was diluted with water, acidified with 2M hydrochloric acid and extracted twice with methylene chloride. The organic layers were each washed with brine, dried over sodium sulfate, combined and concentrated in vacuo to give the crude title acid (27.2 g) which was used directly in Step B.

후처리

  1. temperaturethen cooled
  2. concentrationconcentrated
  3. additionThe residue was diluted with water
  4. extractionextracted twice with methylene chloride
  5. washeach washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ab90bc07387d4fa59b20ba2998402706
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06358979B1

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