Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776532Generated: November 1, 2026

Methanesulfonyl chloride → HCID 5303011, compound

https://huagongshe.com/reaction/1776532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 3-Amino-4-methoxybenzoateHCID 2734814—
SolventPyridineHCID 1049—
ProductHCID 5303011HCID 530301192.5%

Reaction Steps

To a solution of methyl 3-amino-4-methoxybenzoate (0.509 g, 2.81 mmol) in pyridine (10 ml), methanesulfonyl chloride (0.285 ml, 3.65 mmol) was added drop wise and the mixture was stirred at RT for 2 hours. The solvent was removed under vacuum, and the crude was portioned between EtOAc and HCl 1N. The organic phase was dried over Na2SO4 and the solvent was removed. The crude was purified by filtration through a silica gel cartridge (DCM:EtOAc=90:10) to give methyl 4-methoxy-3-(methylsulfonamido)benzoate (0.673 g, 2.60 mmol, 92% yield, MS/ESI+ 259.9 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-f5f000e2cc8f41469d74a50aca36d380
Source noteuspto-grants-2016_02