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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874183Generated: October 30, 2026

Benzylamine → Benzenemethanesulfonamide

https://huagongshe.com/reaction/874183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
ProductBenzenemethanesulfonamideHCID 7831878%

Reaction Conditions

Temperature0 °C

Reaction Steps

Previous intermediate from step 1 was dissolved in 2 mL of dichloromethane and triethylamine (0.035 mL, 0.249 mmol) was added. Solution was cooled to 0° C. and methane sulfonylchloride (0.020 mL, 0.238 mmol) was added. Reaction mixture was warmed to room temperature, stirred overnight, then concentrated under reduced pressure. Residue was purified by silica gel column chromatography (10-90% ethyl acetate in hexanes) to yield the intermediate benzylsulfonamide (35 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980878B2
Source datasetuspto-grants-2015_03
ORD IDord-8b5d5fae4ac54d92affd8ac304b5aea8
Source noteuspto-grants-2015_03