Potassium Carbonate → 1-Tert-butyl 7-ethyl 2-(methoxyacetyl)heptanedioate

HRID 860428노트

반응식

HRID 860428 반응식
[CH3:1][O:2][CH2:3][C:4](=[O:13])[CH2:5][C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7].C(=O)([O-])[O-].[K+].[K+].I[CH2:21][CH2:22][CH2:23][CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26]>CN(C)C=O>[CH3:1][O:2][CH2:3][C:4]([CH:5]([CH2:21][CH2:22][CH2:23][CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])[C:6]([O:8][C:9]([CH3:10])([CH3:12])[CH3:11])=[O:7])=[O:13]

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 4169827Ethyl 5-iodopentanoateHCID 206361091,1-Dimethylethyl 4-methoxy-3-oxobutanoate

생성물 1

HCID 574813401-Tert-butyl 7-ethyl 2-(methoxyacetyl)heptanedioate수율 83.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a suspension of tert-butyl 4-methoxy-3-oxobutanoate (3.09 g) and potassium carbonate (2.50 g) in dimethylformamide (20 mL) was added ethyl 5-iodopentanoate (4.62 g) and the mixture was stirred at ambient temperature for 15 hours. The mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography eluting with a mixture of hexane and ethyl acetate (20:1-5:1) to give 1-tert-butyl 7-ethyl 2-(methoxyacetyl)heptanedioate as colorless oil (4.33 g).

후처리

  1. customThe mixture was partitioned between ethyl acetate and water
  2. customThe organic layer was separated
  3. washwashed with water and brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was purified by silica gel column chromatography
  7. washeluting with a mixture of hexane and ethyl acetate (20:1-5:1)

출처 및 근거

ORD 기록
ord-11821cc61e0c4570b35d91bcdbff0a84
출처 데이터셋
uspto-grants-2006_12
특허 번호
US07153854B2

반응 노트

불러오는 중…