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Acetic Acid → 5,6,7,8-Tetrahydroquinoline-3-carbonitrile

HRID 403248
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HRID 403248 반응식
Cl[C:2]1[C:11]([C:12]#[N:13])=[CH:10][C:9]2[CH2:8][CH2:7][CH2:6][CH2:5][C:4]=2[N:3]=1.O.O.O.C([O-])(=O)C.[Na+].C(O)(=O)C.[OH-].[Na+]>[Zn].O>[N:3]1[C:4]2[CH2:5][CH2:6][CH2:7][CH2:8][C:9]=2[CH:10]=[C:11]([C:12]#[N:13])[CH:2]=1
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참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 37798182-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrileHCID 23665404Sodium Acetate Trihydrate

생성물 1

HCID 5938725,6,7,8-Tetrahydroquinoline-3-carbonitrile수율 53%

시약·촉매·용매 2

HCID 23994Zinc
촉매
HCID 962Water용매

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온도
60 °C

실험 절차

A mixture of commercially available 2-chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile [CAS no 65242-27-5] (1 g, 5.19 mmol), zinc dust (activated) (602 mg, 9.2 mmol) and sodium acetate trihydrate (694 mg, 479 μl, 5.1 mmol) in acetic acid (5.19 g, 4.95 ml, 86.4 mmol) was stirred at 60° C. for 2 hours. Water (2.5 ml) was added and the mixture stirred at 60° C. for another 5 hours. After cooling to 23° C., the mixture was basified with aqueous 1 M NaOH solution, filtered through Celite®, the filtrate extracted with THF, the organic layers dried over Na2SO4 and the solvent evaporated leaving a yellow liquid. The crude material was purified by silica gel flash chromatography with n-heptane/ethyl acetate to give the 5,6,7,8-tetrahydroquinoline-3-carbonitrile as a white solid (433 mg, 53% yield). MS (ISP): m/z=159.1 [(M+H)+].

후처리

  1. stirringthe mixture stirred at 60° C. for another 5 hours
  2. temperatureAfter cooling to 23° C.
  3. filtrationfiltered through Celite®
  4. extractionthe filtrate extracted with THF
  5. dry with materialthe organic layers dried over Na2SO4
  6. customthe solvent evaporated
  7. customleaving a yellow liquid
  8. customThe crude material was purified by silica gel flash chromatography with n-heptane/ethyl acetate

출처 및 근거

ORD 기록
ord-6c4472b0e94243d7b8a936101137f053
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748418B2

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