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Ammonia → HCID 79848845、化合物

HRID 1523301
ノート
印刷プレビュー

反応式

HRID 1523301 の反応式
[O:1]1[CH2:5][CH2:4]/[C:3](=[CH:6]/[C:7]([O:9][CH2:10][CH3:11])=[O:8])/[CH2:2]1.[NH3:12]>O1CCOCC1.CO>[NH2:12][C:3]1([CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:4][CH2:5][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 222AmmoniaHCID 101393316HCID 101393316、化合物

生成物 1

HCID 79848845HCID 79848845、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
150 °C

実験手順

Ethyl (2Z)-dihydrofuran-3(2H)-ylideneacetate (Preparation 36, 1.29 g, 8.25 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 4 hours at 150° C. in a Biotage Initiator™ microwave. The reaction was concentrated in vacuo, but later deemed not to have reached completion. A solution of 7M ammonia in methanol (7 mL) was added and the reaction heated again for 3 hours at 150° C. in the microwave. A further portion of 7M ammonia in methanol (3 mL) was added and the reaction heated for a further 2 hours. 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. concentrationThe reaction was concentrated in vacuo
  2. additionA solution of 7M ammonia in methanol (7 mL) was added
  3. temperaturethe reaction heated again for 3 hours at 150° C. in the microwave
  4. additionA further portion of 7M ammonia in methanol (3 mL) was added
  5. temperaturethe reaction heated for a further 2 hours
  6. concentrationThe reaction was concentrated in vacuo

出典と根拠

ORDレコード
ord-37f18b38cd504054b40ddee565b467b3
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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