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Methanol → HCID 66878002, 화합물

HRID 453712
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HRID 453712 반응식
C([O:5][C:6](=[O:23])[CH2:7][C:8]1([OH:22])[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[CH:10]=[C:11]2[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)(C)(C)C.O[Li].O.O.CO>CCO>[OH:22][C:8]1([CH2:7][C:6]([OH:23])=[O:5])[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[CH:10]=[C:11]2[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 962WaterHCID 168937Lithium hydroxide, monohydrateHCID 77200910HCID 77200910, 화합물

생성물 1

HCID 66878002HCID 66878002, 화합물수율 97.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 4.0 g of rac-(1R*,2R*,4R*)-(2-hydroxy-5-phenyl-bicyclo[2.2.2]oct-5-en-2-yl)-acetic acid tert.-butyl ester in 25 mL EtOH were added 2.1 g of LiOH.H2O, 8 mL H2O and 22 mL MeOH. The reaction mixture was stirred at rt for 3 d and then concentrated. The residue was partitioned between water and Et2O. The aq. layer was separated and acidified with 1N HCl resulting in the formation of a white solid. The solid was filtrated, washed with 5 mL aq. HCl and dried in vacuo to obtain 3.2 g of rac-(1R*,2R*,4R*)-(2-hydroxy-5-phenyl-bicyclo[2.2.2]oct-5-en-2-yl)-acetic acid as white solid.

후처리

  1. concentrationconcentrated
  2. customThe residue was partitioned between water and Et2O
  3. customThe aq. layer was separated
  4. filtrationThe solid was filtrated
  5. washwashed with 5 mL aq. HCl
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-48ba01a66da24db2a17fe235e48fc2dd
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492555B2

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