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Water → 2,4-Dibromothiazole-5-methanol

HRID 577246
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HRID 577246 반응식
[Br:1][C:2]1[S:3][C:4]([CH:8]=[O:9])=[C:5]([Br:7])[N:6]=1.[BH4-].[Na+].O>CO>[Br:1][C:2]1[S:3][C:4]([CH2:8][OH:9])=[C:5]([Br:7])[N:6]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 36928392,4-Dibromo-thiazole-5-carbaldehydeHCID 4311764Sodium borohydride

생성물 1

HCID 100618132,4-Dibromothiazole-5-methanol수율 78.6%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a 0° C. solution of 2,4-dibromo-1,3-thiazole-5-carbaldehyde (3.38 g, 12.3 mmol) in anhydrous methanol (130 mL) was added sodium borohydride (600 mg, 15.9 mmol). The reaction mixture was stirred at room temperature for 3 hours. Water (100 mL) was added, and the mixture was evaporated. The resultant residue was extracted with EtOAc (3×100 mL). The organic extracts were combined, washed with brine (2×100 mL), dried over MgSO4, filtered, evaporated, and dried in vacuo, affording (2,4-dibromo-1,3-thiazol-5-yl)methanol (2.64 g, 77%). The product was used without further purification.

후처리

  1. customthe mixture was evaporated
  2. extractionThe resultant residue was extracted with EtOAc (3×100 mL)
  3. washwashed with brine (2×100 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-580c5175d27e4f3eb3d5f4bc120560d2
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040538B2

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