Trichloro-2-propen-1-ylsilane → HCID 57751175, 화합물

HRID 335677

반응식

HRID 335677 반응식
[C:1]1([CH3:10])[CH:6]=[CH:5][C:4]([S@@](C)=O)=[CH:3][CH:2]=1.C([Si](Cl)(Cl)Cl)C=C.[CH3:18][C:19](=[N:28][NH:29][C:30](=[O:39])[C:31]1[CH:36]=[CH:35][C:34]([CH2:37][CH3:38])=[CH:33][CH:32]=1)[CH2:20][CH2:21][C:22]1C=CC=CC=1>CC(=CC)C.C(Cl)Cl>[CH2:18]([C@@H:19]([NH:28][NH:29][C:30](=[O:39])[C:31]1[CH:32]=[CH:33][C:34]([CH2:37][CH3:38])=[CH:35][CH:36]=1)[CH2:20][CH:21]=[CH2:22])[CH2:10][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

참가 물질

6

반응물 3

HCID 7867Trichloro-2-propen-1-ylsilaneHCID 10913262(R)-Methyl p-tolylsulfoxideHCID 850298514-Ethyl-benzoic acid (1-methyl-3-phenyl-propylidene)hydrazide

생성물 1

HCID 57751175HCID 57751175, 화합물수율 41.4%

시약·촉매·용매 2

HCID 6344Dichloromethane용매2회HCID 105532-Methyl-2-butene용매

실험 절차

(R)-(+)-methyl p-tolyl sulfoxide (0.5 g, 3.21 mmoles) and tetrabutylammonium triphenyl-difluorosilicate (TBAT) (0.12 g, 0.214 mmoles) were dissolved in 0.038 mL of 2-methyl-2-butene and 2.4 mL of anhydrous methylene chloride under nitrogen and with magnetic stirring. Allyltrichlorosilane (0.23 mL, 1.61 mmoles) was added at −78° C. and the reaction was stirred for 15 minutes. 4-ethyl-benzoic acid (1-methyl-3-phenyl-propylidene)hydrazide (0.3 g, 1.07 mmoles) was dissolved in 11.6 mL of anhydrous methylene chloride and added to the reaction over a period of 30 minutes. The reaction mixture was stirred for 5 hours under nitrogen and maintained at −78° C. to −70° C., with TLC monitoring. The reaction was quenched with 1.5 mL triethylamine and 3 mL anhydrous methanol at −78° C. Brine was then added and the mixture was allowed to warm to room temperature. The organic layer was removed, combined with three methylene chloride extractions, and dried over sodium sulfate. The solvent was evaporated, and the crude mixture was purified by flash chromatography using a step gradient of 2:1 and 1:1 pentane:ethyl acetate. Purified (R)-4-ethyl-benzoic acid N′-(1-phenethyl-but-3-enyl)-hydrazide was obtained as a clear oil (0.145 g, 41.4% yield, 57.6% ee by chiral HPLC on Chiralcel ADH). Rf=0.50 (1:1 EtOAc:n-hexane); 1H NMR (400 MHz, CDCl3) δ 7.64-7.13 (m, 9H), 5.91 (m, 1H), 5.15 (t, J=28.0 Hz, 2H), 3.12 (m, 1H), 2.76-2.63 (m, 4H), 2.38-2.24 (m, 2H), 1.88-1.74 (m, 2H), 1.23 (t, J=8.0 Hz, 3H).

후처리

  1. additionadded to the reaction over a period of 30 minutes
  2. stirringThe reaction mixture was stirred for 5 hours under nitrogen
  3. temperaturemaintained at −78° C. to −70° C., with TLC monitoring
  4. customThe reaction was quenched with 1.5 mL triethylamine and 3 mL anhydrous methanol at −78° C
  5. additionBrine was then added
  6. customThe organic layer was removed
  7. extractioncombined with three methylene chloride extractions
  8. dry with materialdried over sodium sulfate
  9. customThe solvent was evaporated
  10. customthe crude mixture was purified by flash chromatography

출처 및 근거

ORD 기록
ord-18b68b1291ea45f3a2eaa2d6888cf916
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08884060B2

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