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Acetic Acid → Ethyl 2-cyano-4,4-dimethylpent-2-enoate

HRID 375102
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HRID 375102 반응식
[CH3:1][C:2]([CH:5]=O)([CH3:4])[CH3:3].[CH2:7]([O:9][C:10](=[O:14])[CH2:11][C:12]#[N:13])[CH3:8].C(O)(=O)C.N1C=CC=CC=1>Cl>[CH2:7]([O:9][C:10](=[O:14])[C:11]([C:12]#[N:13])=[CH:1][C:2]([CH3:5])([CH3:4])[CH3:3])[CH3:8]
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참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 1049PyridineHCID 7764Ethyl cyanoacetateHCID 12417Pivalaldehyde2회

생성물 1

HCID 53661853Ethyl 2-cyano-4,4-dimethylpent-2-enoate수율 73.2%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A mixture of pivaldehyde (5.00 g, 58 mmol), ethylcyanoacetate (6.60g, 58.3 mmol), acetic acid (3.50 g, 58.3 mmol) and pyridine (4.60 g, 58.2 mmol) was heated at reflux for 1 h. A second portion of pivaldehyde (5.00 g, 58 mmol) was added. The refluxing of the mixture was continued for 18h. After cooling, the mixture was poured into 1N aqueous HCl (50 mL). The resulting mixture was extracted with EtOAc (3×50 mL). The combined organic layers, were washed with 1N aqueous HCl, dried (MgSO4) and concentrated to give a colorless oil. The oil was purified by flash chromatography on SiO2 using hexane-EtOAc (9:1) as the eluant to give 2-cyano-4,4-dimethyl-2-pentenoic acid ethyl ester as a colorless oil (7.69 g, 73 % yield).

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 1 h
  3. temperatureThe refluxing of the mixture
  4. temperatureAfter cooling
  5. extractionThe resulting mixture was extracted with EtOAc (3×50 mL)
  6. washThe combined organic layers, were washed with 1N aqueous HCl
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated
  9. customto give a colorless oil
  10. customThe oil was purified by flash chromatography on SiO2

출처 및 근거

ORD 기록
ord-3a447c8db62f4639b43b05ce57a7ad71
출처 데이터셋
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05484771

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