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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776540Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86679496, compound

https://huagongshe.com/reaction/1776540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantPhenylmethyl 3-amino-4-methoxybenzoateHCID 54195745—
SolventHydrochloric AcidHCID 313—
ProductHCID 86679496HCID 8667949663.2%

Reaction Steps

Benzyl 3-amino-4-methoxybenzoate (300 mg, 1.17 mmol) was dissolved in Py (5 ml). Methanesulfonyl chloride (140 mg, 1.22 mmol) was added at 0° C. and under Argon atmosphere. The mixture was stirred at RT for 1 hour, then it was diluted with HCl 1N and extracted with EtOAc. The organic phase was washed with HCl 1M, dried over Na2SO4 and concentrated under vacuum to give benzyl 4-methoxy-3-(methylsulfonamido)benzoate (247 mg, 63.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-2a69283b5dea4a0ba6a6c79067302f0c
Source noteuspto-grants-2016_02