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Sodium Chloride → methyl (1R,2R)-2-(hydroxymethyl)cyclopropane-1-carboxylate

HRID 456512
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HRID 456512 반응식
[CH3:1][O:2][C:3]([C@@H:5]1[CH2:7][C@H:6]1[C:8](O)=[O:9])=[O:4].B(OC)(OC)OC.[Cl-].[Na+]>O1CCCC1>[CH3:1][O:2][C:3]([C@@H:5]1[CH2:7][C@H:6]1[CH2:8][OH:9])=[O:4]
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참가 물질

5

반응물 3

HCID 5234Sodium ChlorideHCID 8470Trimethyl borateHCID 12510972rac-(1R,2R)-2-(methoxycarbonyl)cyclopropane-1-carboxylic acid

생성물 1

HCID 10931461methyl (1R,2R)-2-(hydroxymethyl)cyclopropane-1-carboxylate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Add borane-methyl sulfide complex (177 mL, 0.354 mol), slowly, by means of a dropping funnel, to a stirring solution of trans-cyclopropane-1,2-dicarboxylic acid monomethyl ester (Example 3a) (25.5 g, 0.177 mol), trimethyl borate (60.3 mL, 0.531 mol) and tetrahydrofuran (150 mL) at 0° C. After complete addition, allow the reaction to come to ambient temperature and stir for 2 h more. Pour the reaction mixture into a stirring solution of 50% aqueous sodium chloride solution (1.5 L)-concentrated HCl (10 mL). Extract the mixture with ethyl acetate (EtOAc) (3 times), combine the extracts, dry (Na2SO4) and concentrate the solvent to obtain a colorless oil: 22.6 g.

후처리

  1. additionAdd borane-methyl sulfide complex (177 mL, 0.354 mol)
  2. customat 0° C
  3. additionAfter complete addition
  4. customthe reaction
  5. customto come to ambient temperature
  6. extractionExtract the mixture with ethyl acetate (EtOAc) (3 times)
  7. dry with materialdry (Na2SO4)
  8. concentrationconcentrate the solvent
  9. customto obtain a colorless oil

출처 및 근거

ORD 기록
ord-d0f952f9aeea4e51aae9613756a290f2
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07186724B2

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