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2-Chloroacrylonitrile → HCID 13361513, 화합물

HRID 1788749
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HRID 1788749 반응식
[C:1]([NH:4][C@@H:5]1[CH2:9][CH2:8][CH2:7][C@H:6]1[Hg]Cl)(=[O:3])[CH3:2].[Cl:12][C:13](=[CH2:16])[C:14]#[N:15].[BH4-].[Na+]>C(O)C>[C:1]([NH:4][C@@H:5]1[CH2:9][CH2:8][CH2:7][C@H:6]1[CH2:16][CH:13]([Cl:12])[C:14]#[N:15])(=[O:3])[CH3:2]
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참가 물질

5

반응물 3

HCID 701982-ChloroacrylonitrileHCID 4311764Sodium borohydrideHCID 12257138HCID 12257138, 화합물

생성물 1

HCID 13361513HCID 13361513, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

16.1 g of trans-1-acetamido-2-chloromercuriocyclopentane are suspended in 200 ml of ethanol. 10.7 ml of 2-chloroacrylonitrile are added, followed by 1.7 g of sodium borohydride in 40 ml of ethanol as rapidly as possible while cooling in ice. After 1 hour at room temperature, the mixture is filtered with suction through kieselguhr, the filtrate is evaporated, the residue is taken up with methylene chloride, this solution is washed twice with 1N sodium hydroxide solution, and the organic phase is dried over sodium sulfate and evaporated. Chromatography on silica gel (mobile phase ethyl acetate) produces 2.2 g of crystalline product, melting point 114°-117° C.

후처리

  1. temperaturewhile cooling in ice
  2. filtrationthe mixture is filtered with suction through kieselguhr
  3. customthe filtrate is evaporated
  4. washthis solution is washed twice with 1N sodium hydroxide solution
  5. dry with materialthe organic phase is dried over sodium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-d90b8545ce624e38851dac4a9f3f4f7e
출처 데이터셋
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04684662

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