Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53668Generated: October 29, 2026

Sodium hydride → 2-Bromo-N-Methylsulfonylacetamide

https://huagongshe.com/reaction/53668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBromoacetyl bromideHCID 61147—
ReactantMethanesulfonamideHCID 72879—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-N-MethylsulfonylacetamideHCID 262944—

Reaction Steps

Sodium hydride (1.68 g×60% ) was added to a stirred solution of methanesulfonamide (2.0 g) in dry tetrahydrofuran (20 ml) at room temperature. The resulting solution was stirred at room temperature for 1 hour, as which time it was treated with a solution of bromoacetyl bromide (4.2 g) in dry tetrahydrofuran (10 ml). After 1 hour the solvent was removed under reduced pressure and the residue taken up in water and acidified to pH3. The acidic solution was extracted into ethyl acetate, dried (MgSO4), filtered and the solvent removed under reduced pressure. Recrystallisation from isopropanol afforded the product as white needles: mp 112°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620989
Source datasetuspto-grants-1997_04
ORD IDord-575b933edd854cfcb80aab968d02232c
Source noteuspto-grants-1997_04