Lithium borohydride → Tert-Butyl(1-(Hydroxymethyl)cyclopropyl)methylcarbamate

HRID 496061ノート

反応式

HRID 496061 の反応式
[BH4-].[Li+].[C:3]([O:7][C:8]([N:10]([CH3:18])[C:11]1([C:14](OC)=[O:15])[CH2:13][CH2:12]1)=[O:9])([CH3:6])([CH3:5])[CH3:4]>O1CCCC1.CCOCC>[OH:15][CH2:14][C:11]1([N:10]([CH3:18])[C:8](=[O:9])[O:7][C:3]([CH3:4])([CH3:5])[CH3:6])[CH2:12][CH2:13]1

参加物

5

反応物 2

HCID 4148881Lithium borohydrideHCID 22325133Methyl 1-[[(1,1-dimethylethoxy)carbonyl]methylamino]cyclopropanecarboxylate

生成物 1

HCID 52988048Tert-Butyl(1-(Hydroxymethyl)cyclopropyl)methylcarbamate

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

100 ml of a 2M solution of lithium borohydride in tetrahydrofuran is added to a solution of 23 g of the compound obtained in Step 2 in 100 ml of tetrahydrofuran. After stirring for 20 hours at ambient temperature and then refluxing for 8 hours, the reaction mixture is cooled to 0° C., hydrolysed, diluted with ether, separated, dried and concentrated. Chromatography of the residue over silica gel (dichloromethane/tetrahydrofuran: 95/5) allows the expected product to be isolated.

後処理

  1. temperaturerefluxing for 8 hours
  2. temperaturethe reaction mixture is cooled to 0° C.
  3. customseparated
  4. customdried
  5. concentrationconcentrated
  6. customto be isolated

出典と根拠

ORDレコード
ord-5fb77eb273774e15a4e64a3b0abb9ee1
出典データセット
uspto-grants-2005_09
特許番号
US06943184B2

反応ノート

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