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2,3-Dihydroxybutanedioic Acid → Ethyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](hydroxy)acetate

HRID 1881890
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HRID 1881890 반응식
[BH4-].[Na+].C(O)(=O)C(C(C(O)=O)O)O.[O:13]1[CH2:17][CH2:16][O:15][CH:14]1[C:18]1[S:19][C:20]([C:23](=[O:29])[C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:21][N:22]=1>O1CCCC1>[O:15]1[CH2:16][CH2:17][O:13][CH:14]1[C:18]1[S:19][C:20]([CH:23]([OH:29])[C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:21][N:22]=1
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참가 물질

5

반응물 3

HCID 8752,3-Dihydroxybutanedioic AcidHCID 4311764Sodium borohydrideHCID 59331559Ethyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](oxo)acetate

생성물 1

HCID 59331299Ethyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](hydroxy)acetate수율 80%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
80 °C

실험 절차

A suspension of sodium borohydride (6.18 g) and DL-tartaric acid (24.5 g) in tetrahydrofuran (250 mL) was stirred at 80° C. for 2 hr. The reaction mixture was cooled to 0° C., ethyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](oxo)acetate (10.49 g) was added, and the mixture was stirred at room temperature for 2 days. The reaction mixture was slowly poured into ice (100 g), and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO9) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (8.43 g, yield 80%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (4:1, volume ratio). MS: 260 (MH+).

후처리

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. stirringthe mixture was stirred at room temperature for 2 days
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe ethyl acetate layer was washed with saturated brine
  5. dry with materialdried (MgSO9)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c2844104650542ceadff28de21895c01
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318746B2

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