Tri-o-tolylphosphine → Tert-butyl 2,6-dichlorophenethyl(3-(2-oxopropyl)benzyl)carbamate

HRID 553280

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HRID 553280 반응식
[C:1]([O:5][C:6](=[O:26])[N:7]([CH2:16][CH2:17][C:18]1[C:23]([Cl:24])=[CH:22][CH:21]=[CH:20][C:19]=1[Cl:25])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11](I)[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].C[O-].[CH2:29]([Sn+](CCCC)CCCC)[CH2:30][CH2:31]C.C(OC=CC(=C)C)(=[O:44])C.C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C>C1(C)C=CC=CC=1>[C:1]([O:5][C:6](=[O:26])[N:7]([CH2:16][CH2:17][C:18]1[C:23]([Cl:24])=[CH:22][CH:21]=[CH:20][C:19]=1[Cl:25])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:29][C:30](=[O:44])[CH3:31])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2]

참가 물질

6

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온도
100 °C

실험 절차

[2-(2,6-Dichloro-phenyl)-ethyl]-(3-iodo-benzyl)-carbamic acid tert-butyl ester (Example 14, step b) (500 mg), tributyltin methoxide (350 μL), isoprenyl acetate (170 μL), tri-o-tolylphosphine (30 mg) and toluene (20 mL) were charged to a flask and the solution degassed with nitrogen for 5 minutes. Palladium acetate (10 mg) was added and the resultant mixture heated to 100° C., under nitrogen, for 3 hours. On cooling, potassium fluoride (580 mg) in water (3 mL) was added, stir at room temperature for 18 hours. The solids were filtered off, and the filter cake washed with ethyl acetate. The filtrate was evaporated and purified on silica, eluting with a gradient of iso-hexane/ethyl acetate [4:1 to 2:1], to give the subtitle product as an oil (230 mg).

후처리

  1. customthe solution degassed with nitrogen for 5 minutes
  2. additionPalladium acetate (10 mg) was added
  3. temperatureOn cooling
  4. additionpotassium fluoride (580 mg) in water (3 mL) was added
  5. filtrationThe solids were filtered off
  6. washthe filter cake washed with ethyl acetate
  7. customThe filtrate was evaporated
  8. custompurified on silica
  9. washeluting with a gradient of iso-hexane/ethyl acetate [4:1 to 2:1]

출처 및 근거

ORD 기록
ord-ad8f92d1c2294bb6a3c2dd8618b77800
출처 데이터셋
uspto-grants-2011_05
특허 번호
US07951954B2

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