Water → (3-Chloropyridin-4-yl)methanol

HRID 577253

反応式

HRID 577253 の反応式
[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH:8]=[O:9].[BH4-].[Na+].O>CO>[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8][OH:9]

参加物

5

実験手順

To a 0° C. solution of 3-chloropyridine-4-carbaldehyde (1.08 g, 7.5 mmol) in anhydrous methanol (75 mL) was added sodium borohydride (405 mg, 10.7 mmol). The reaction mixture was stirred at room temperature for 1.5 hours. Water (75 mL) was added, and the reaction mixture was evaporated. The resultant residue was extracted with EtOAc (3×50 mL). The organic extracts were combined, washed with brine (2×100 mL), dried over MgSO4, filtered, evaporated, and dried in vacuo, affording (3-chloropyridin-4-yl)methanol (1.0 g, 96%). The product was used in the next step without further purification.

後処理

  1. customthe reaction mixture was evaporated
  2. extractionThe resultant residue was extracted with EtOAc (3×50 mL)
  3. washwashed with brine (2×100 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customdried in vacuo

出典と根拠

ORDレコード
ord-300ad6f283da4223b84787cdea6d4bf2
出典データセット
uspto-grants-2015_05
特許番号
US09040538B2

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