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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518951Generated: October 25, 2026

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

https://huagongshe.com/reaction/1518951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriethylsilaneHCID 12052—
ReactantN-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamideHCID 28560458—
ReactantHCID 178418416HCID 178418416—
SolventDimethylformamideHCID 6228—
Product(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamideHCID 86691231—

Reaction Conditions

Temperature90 °C

Reaction Steps

Mix 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. Then charge the reactor with carbon monoxide (50 psi) and stir the mixture at 90° C. for 15 hours. Cool the reactor to ambient temperature, filter over Celite® pad and wash with DCM (150 mL). Sequentially wash the filtrate with water then brine (2×80 mL). Concentrate the organic filtrate under vacuum to obtain the residue as an orange oil. Purify the crude by silica gel flash chromatography eluting with hexane/ethyl acetate (0 to 30% ethyl acetate) 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 numberUS09073856B2
Source datasetuspto-grants-2015_07
ORD IDord-948b7050c31d4a639642eafa35ff2efa
Source noteuspto-grants-2015_07