Acetic Acid → 2-Cyano-4,4,8-trimethyl-non-2-enoic acid benzyl ester

HRID 28451

反応式

HRID 28451 の反応式
[CH3:1][C:2]([CH3:11])([CH2:5][CH2:6][CH2:7][CH:8]([CH3:10])[CH3:9])[CH:3]=O.N1CCCCC1.[C:18]([CH2:20][C:21]([O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22])#[N:19].C(O)(=O)C.Cl>C1(C)C=CC=CC=1>[CH2:24]([O:23][C:21](=[O:22])[C:20]([C:18]#[N:19])=[CH:3][C:2]([CH3:11])([CH3:1])[CH2:5][CH2:6][CH2:7][CH:8]([CH3:10])[CH3:9])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1

参加物

7

反応物 5

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 8082PiperidineHCID 560818Benzyl 2-cyanoacetateHCID 219436612,2,6-Trimethyl-heptanal

生成物 1

HCID 688724612-Cyano-4,4,8-trimethyl-non-2-enoic acid benzyl ester収率 61.6%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a mixture of 2,2,6-Trimethyl-heptanal (1.05 g, 6.73 mmol), piperidine (0.19 mL, 2.01 mmol) and benzyl cyanoacetate (1.29 g, 7.4 mmol) in toluene (50 mL) was added glacial acetic acid (0.72 g, 12.1 mmol). The flask was fitted with a Dean-Stark trap, and the mixture was heated at reflux for 18. The mixture was cooled, treated with dilute HCl, and the layers were separated. The organics were washed with a saturated sodium bicarbonate solution followed by brine, and dried (MgSO4), filtered and concentrated. The residual oil was purified by silica gel chromatography (98/2 hexane/EtOAc) to give 1.3 g of 2-Cyano-4,4,8-trimethyl-non-2-enoic acid benzyl ester m/z 314 (M+).

後処理

  1. customThe flask was fitted with a Dean-Stark trap
  2. temperaturethe mixture was heated
  3. temperatureat reflux for 18
  4. temperatureThe mixture was cooled
  5. customthe layers were separated
  6. washThe organics were washed with a saturated sodium bicarbonate solution
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe residual oil was purified by silica gel chromatography (98/2 hexane/EtOAc)

出典と根拠

ORDレコード
ord-9dc558629ce14142bf4d4ee6b3962698
出典データセット
uspto-grants-2008_09
特許番号
US07419981B2

関連ノート

読み込み中…