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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamide | HCID 28560458 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Triethylsilane | HCID 12052 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamide | HCID 86691231 | 70.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575352B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-f3bde30ae8e64a0fbe61c42f787704c8 |
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| Source note | uspto-grants-2013_11 |
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