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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038216Generated: October 25, 2026

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

https://huagongshe.com/reaction/2038216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantN-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamideHCID 28560458—
ReactantHCID 178418416HCID 178418416—
CatalystTriethylsilaneHCID 12052—
SolventDimethylformamideHCID 6228—
Product(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamideHCID 8669123170.4%

Reaction Steps

Charge a 300 mL PARR reactor with 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). Add triethylsilane (11.6 mL, 0.72 mmol) and purge the reactor with carbon monoxide three times. Pressurize the PARR reactor with carbon monoxide (50 psi) and stir the mixture at 90° C. for 15 hours. Cool the reactor to ambient temperature; filter through 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 provide an orange oil residue. Purify the residue by silica gel flash chromatography eluting with hexane/EtOAc (0 to 30% EtAc) to provide the title compound (5.6 g, 70%, ee>98%). MS (m/z): 228 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575352B2
Source datasetuspto-grants-2013_11
ORD IDord-f3bde30ae8e64a0fbe61c42f787704c8
Source noteuspto-grants-2013_11