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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamide | HCID 28560458 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamide | HCID 86691231 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073856B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-948b7050c31d4a639642eafa35ff2efa |
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| Source note | uspto-grants-2015_07 |
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