참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | Triethylsilane | HCID 12052 | — |
| 반응물 | N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamide | HCID 28560458 | — |
| 반응물 | HCID 178418416 | HCID 178418416 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamide | HCID 86691231 | — |
반응 단계
Combine N-[(1R)-1-(4-bromophenyl)ethyl]-methanesulfonamide (10 g, 35 mmol), (1,1′-bis(diphenylphosphino)-ferrocene)palladium(II) chloride (733 mg, 0.9 mmol), sodium carbonate (3.81 g, 35 mmol) and DMF (50 mL) in a 300 mL PARR reactor. Add triethylsilane (11.6 mL, 0.72 mmol) and purge the reactor with carbon monoxide three times. Charge the reactor with carbon monoxide (50 psi) and stir the mixture at 90° C. for 15 h. Cool the reactor to ambient temperature; open; filter mixture through a Celite® pad; and wash the pad with DCM (150 mL). Sequentially wash the filtrate with water then brine (2×80 mL). Concentrate the organic phase under reduced pressure to obtain the residue as an orange oil. Purify the orange oil by silica gel flash chromatography eluting with hexane/EtOAc (0 to 30% EtOAc) to provide the title compound (5.6 g, 70%, ee>98%). MS (m/z): 228 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08993568B2 |
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| 출처 데이터셋 | uspto-grants-2015_03 |
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| ORD ID | ord-e84f96b910b44827b4ff26260fbc4ed5 |
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| 출처 메모 | uspto-grants-2015_03 |
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