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Sodium Thiosulfate → Ethyl 6-oxohexanoate

HRID 915715
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HRID 915715 반응식
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8].CC1(C)N([O])C(C)(C)CCC1.C(O)(=O)C.C(O)(=O)C.IC1C=CC=CC=1.[O-]S([O-])(=S)=O.[Na+].[Na+]>C(Cl)Cl>[CH:2]([CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:1]
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참가 물질

6

반응물 4

HCID 24477Sodium ThiosulfateHCID 357781Ethyl 6-hydroxyhexanoateHCID 2724126TempoHCID 12217721Iodo benzene diacetate

생성물 1

HCID 11171124Ethyl 6-oxohexanoate

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a flask containing ethyl 6-hydroxyhexanoate (4.07 mL, 25.0 mmol) in CH2Cl2 (25 mL) was added TEMPO (391 mg, 2.50 mmol) followed by iodobenzene diacetate (8.86 g, 27.5 mmol). The reaction was stirred 2 hours and then diluted with CH2Cl2 (100 mL). Saturated aqueous solution of Na2S2O3 (100 mL) was added and extracted with CH2Cl2 (3×50 mL). The combined organics were washed with saturated aqueous NaHCO3 (150 mL) and brine (150 mL), dried over Na2SO4, and concentrated in vacuo. The resulting residue was purified by silica gel chromatography (20-40% Et2O/pentanes) to provide the title compound, which was identical to the reported literature compound. (See: Taber, D. F.; Teng, D. (2002) J. Org. Chem., 67: 1607.)

후처리

  1. extractionextracted with CH2Cl2 (3×50 mL)
  2. washThe combined organics were washed with saturated aqueous NaHCO3 (150 mL) and brine (150 mL)
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. customThe resulting residue was purified by silica gel chromatography (20-40% Et2O/pentanes)

출처 및 근거

ORD 기록
ord-bfc297eb862847fda78ae0a92e6bc697
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07265249B2

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