Oxalic Acid → (E)-3-{2-(4-fluoro-3-methylphenyl)-4-(pyrrolidin-1-yl)-6,6-dimethylcyclohex-1-en-1-yl}propenal

HRID 359566노트

반응식

HRID 359566 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:13][CH:12]([N:14]3[CH2:18][CH2:17][CH2:16][CH2:15]3)[CH2:11][C:10]([CH3:20])([CH3:19])[C:9]=2[CH:21]=O)=[CH:4][C:3]=1[CH3:23].[Li+].CC([N-]C(C)C)C.C(=NC1CCCCC1)C.[C:41]([OH:46])(=O)[C:42](O)=O>CCOCC.O.C([O-])(O)=O.[Na+]>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:13][CH:12]([N:14]3[CH2:15][CH2:16][CH2:17][CH2:18]3)[CH2:11][C:10]([CH3:19])([CH3:20])[C:9]=2/[CH:21]=[CH:42]/[CH:41]=[O:46])=[CH:4][C:3]=1[CH3:23]

참가 물질

8

반응물 4

HCID 971Oxalic AcidHCID 2724682Lithium diisopropylamideHCID 10964544N-cyclohexylethanimineHCID 150569662-(4-Fluoro-3-methylphenyl)-4-(pyrrolidin-1-yl)-6, 6-dimethylcyclohex-1-en-1-carboxaldehyde

생성물 1

HCID 15056967(E)-3-{2-(4-fluoro-3-methylphenyl)-4-(pyrrolidin-1-yl)-6,6-dimethylcyclohex-1-en-1-yl}propenal수율 54.9%

시약·촉매·용매 3

HCID 962Water용매HCID 3283Diethyl Ether용매2회HCID 516892Sodium Bicarbonate용매

실험 절차

In a manner similar to Scheme I, 32 (3.80 g, 12.1 mmol) was treated with the LDA-derived anion of ethylidenecyclohexylamine (2.90 g, 23.2 mmol) in anhydrous ether. Workup and purification of the residue by HPLC. using 1% Et3N in 10:l hexanes:EtOAc as eluent provided the dieneimine (2.4 g). The imine and oxalic acid (10 g) in 40 mL H2O was heated at 100° C. for 2 h, cooled, diluted with saturated NaHCO3 and ether. The organic layer was washed with H2O and brine and dried (MgSO4). Removal of volatiles in vacuo provided 2.27 g of gum which was taken forward without further purification.

후처리

  1. customWorkup and purification of the residue by HPLC
  2. customl hexanes:EtOAc as eluent provided the dieneimine (2.4 g)
  3. temperaturecooled
  4. washThe organic layer was washed with H2O and brine
  5. dry with materialdried (MgSO4)
  6. customRemoval of volatiles in vacuo

출처 및 근거

ORD 기록
ord-7d12770473ea4395909f18527ad57bb1
출처 데이터셋
uspto-grants-1991_03
특허 번호
US05001144

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