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Ammonia → HCID 79848845, 화합물

HRID 1523301
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HRID 1523301 반응식
[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
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참가 물질

5

반응물 2

HCID 222AmmoniaHCID 101393316HCID 101393316, 화합물

생성물 1

HCID 79848845HCID 79848845, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 312751,4-Dioxane용매

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온도
150 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-37f18b38cd504054b40ddee565b467b3
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09079878B2

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