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HRID 1483024作成日:2026年10月25日

Sodium Carbonate → (R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamide

https://huagongshe.com/reaction/1483024

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物TriethylsilaneHCID 12052—
反応物N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamideHCID 28560458—
反応物HCID 178418416HCID 178418416—
溶媒DimethylformamideHCID 6228—
生成物(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamideHCID 86691231—

反応条件

温度90 °C

反応手順

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); seal; and stir the mixture at 90° C. for 15 hours. Cool the reactor to ambient temperature; filter the resulting mixture over Celite® pad; and wash the pad with DCM (150 mL). Collect the filtrate and sequentially wash the filtrate with water then brine (2×80 mL). Concentrate the organic filtrate under reduced pressure to obtain the residue as an orange oil. Purify 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09416138B2
出典データセットuspto-grants-2016_08
ORD IDord-77e918318dff4ba7a06fb4c1fea5dc27
出典メモuspto-grants-2016_08