Ammonium Chloride → 4-Chloro-3-quinolinemethanol

HRID 576964ノート

反応式

HRID 576964 の反応式
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[CH:12]=[O:13].[BH4-].[Na+].[Cl-].[NH4+]>CO>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[CH2:12][OH:13]

参加物

5

反応物 3

HCID 25517Ammonium ChlorideHCID 14780304-chloroquinoline-3-carbaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 2243974-Chloro-3-quinolinemethanol収率 85%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a 0° C. solution of 4-chloroquinoline-3-carbaldehyde (1.2 g, 6.3 mmol) in anhydrous methanol (20 mL) was added sodium borohydride (250 mg, 6.6 mmol). The reaction mixture was stirred at room temperature for 3 hours. Saturated ammonium chloride solution (20 mL) was added. The resultant mixture was extracted with dichloromethane (2×20 mL). The organic extracts were combined, dried over MgSO4, filtered, evaporated, and dried in vacuo, affording (4-chloroquinolin-3-yl)methanol (1.0 g, 85% yield). The product was used without further purification.

後処理

  1. extractionThe resultant mixture was extracted with dichloromethane (2×20 mL)
  2. dry with materialdried over MgSO4
  3. filtrationfiltered
  4. customevaporated
  5. customdried in vacuo

出典と根拠

ORDレコード
ord-ce9a82bdb57f45488d67c1fa50bcee54
出典データセット
uspto-grants-2015_05
特許番号
US09040538B2

反応ノート

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