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Ammonia → Ethyl 2-(3-aminooxan-3-YL)acetate

HRID 1523302
ノート
印刷プレビュー

反応式

HRID 1523302 の反応式
[O:1]1[CH2:6][CH2:5][CH2:4]/[C:3](=[CH:7]/[C:8]([O:10][CH2:11][CH3:12])=[O:9])/[CH2:2]1.[NH3:13]>O1CCOCC1.CO>[NH2:13][C:3]1([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:5][CH2:6][O:1][CH2:2]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 222Ammonia2 回HCID 11768987HCID 11768987、化合物

生成物 1

HCID 79849317Ethyl 2-(3-aminooxan-3-YL)acetate

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回HCID 312751,4-Dioxane溶媒

反応条件

温度
150 °C

実験手順

Ethyl (2Z)-dihydro-2H-pyran-3(4H)-ylideneacetate (Preparation 37, 1.21 g, 7.11 mmol) was stirred in 1,4-dioxane (7 mL) in a microwave vial. A solution of 7M ammonia in methanol (5 mL) was added and the reaction heated for 3 hours at 150° C. in a Biotage Initiator™ microwave. A further solution of 7M ammonia in methanol (2 mL) was added and the reaction heated again for 2 hours at 150° C. in the microwave. The reaction was concentrated in vacuo and the residue dissolved in a further portion of 7M ammonia in methanol (10 mL) and heated for a further 5 hours at 150° C. in the microwave. The reaction was concentrated in vacuo to afford the title compound along with the methyl ester where trans-esterification had occurred. The material was used without further purification in the next step.

後処理

  1. temperaturethe reaction heated again for 2 hours at 150° C. in the microwave
  2. concentrationThe reaction was concentrated in vacuo
  3. dissolutionthe residue dissolved in a further portion of 7M ammonia in methanol (10 mL)
  4. temperatureheated for a further 5 hours at 150° C. in the microwave
  5. concentrationThe reaction was concentrated in vacuo

出典と根拠

ORDレコード
ord-2151be9f41ed4790a9cd90954504704e
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09079878B2

反応ノート

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