Acetone → Ethyl 2-((propan-2-yl)amino)acetate

HRID 716296

反応式

HRID 716296 の反応式
Cl.[NH2:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[CH3:9][C:10]([CH3:12])=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+]>C1COCC1.C(OCC)(=O)C.O.C(O)(=O)C>[CH:10]([NH:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5])([CH3:12])[CH3:9]

参加物

9

実験手順

To a suspension of ethyl 2-aminoacetate hydrochloride (20 g, 143.28 mmol) in THF (400 mL) was added glacial acetic acid (20 mL) followed by acetone (11.59 mL, 151.62 mmol). The reaction was stirred 30 min at room temperature. Sodium triacetoxyborohydride (60.73 g, 286.56 mmol) was added over the course of one hour. The reaction was poured slowly into a vigorously stirred biphasic mixture of water (300 mL) and ethyl acetate (800 mL). The aqueous layer was adjusted to pH 13 using a solution of 50% (weight) NaOH. The mixture was stirred 30 min and poured into a separatory funnel. The organic layer was collected and the aqueous layer was back extracted with ethyl acetate (3×200 mL). The organic layers were combined, washed with brine (300 mL), dried with sodium sulfate, and concentrated to yield the title compound (17.6 g, 85%) as a translucent oil which was used in the next step without further purification. [M+H] calc'd for C7H15NO2, 146. found, 146.

後処理

  1. stirringThe mixture was stirred 30 min
  2. additionpoured into a separatory funnel
  3. customThe organic layer was collected
  4. extractionthe aqueous layer was back extracted with ethyl acetate (3×200 mL)
  5. washwashed with brine (300 mL)
  6. dry with materialdried with sodium sulfate
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-8aa297fada614315ac17fdf39e9d0a71
出典データセット
uspto-grants-2015_11
特許番号
US09187497B2

関連ノート

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