Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308355Generated: October 31, 2026

Diethyl Ether → HCID 8823780, compound

https://huagongshe.com/reaction/2308355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantBenzoic acid, 2-(chlorosulfonyl)-, methyl esterHCID 117830—
SolventDichloromethaneHCID 6344—
ProductHCID 8823780HCID 8823780—

Reaction Steps

Methyl 2-(chlorosulfonyl)-benzoate (2.25 g, 8.73 mmol) in methylene chloride (20 mL) was added dropwise to a solution of ethyl 3-aminobenzoate (1.44 g, 8.73 mmol) and triethylamine (1.21 mL, 8.73 mmol) in methylene chloride (10 mL) at 0° C. The reaction was allowed to warm to room temperature and stirred overnight. The reaction mixture was washed with water (20 mL), aqueous HCl (1 M, 20 mL) and aqueous NaOH (1 M, 20 mL), dried (MgSO4—, filtered and concentrated in vacuo to give an orange oil. Trituration with ethyl ether gave N-(3′-carboethoxyphenyl)-2-(carbomethoxy)benzenesulfonamide as white solid. 1H NMR (200 MHz, CDCl3): δ 1.31, t, J=6.0 Hz, 3H; 4.00, s, 3H; 4.29, q, J=6.0 Hz, 2H; 7.23-7.61, m, 5H; 7.66-7.92, m, 3H; 8.26, br s , 1H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06835753B2
Source datasetuspto-grants-2004_12
ORD IDord-627264e7e22a43dda5b62ca5cdcc8366
Source noteuspto-grants-2004_12