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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386711Generated: October 26, 2026

Benzoic acid, 3-(chlorosulfonyl)-, methyl ester → HCID 66797535, compound

https://huagongshe.com/reaction/386711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 3-(chlorosulfonyl)-, methyl esterHCID 113339—
Reactant1366068-12-3HCID 66797588—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 66797535HCID 66797535—

Reaction Steps

A solution of 1-aminomethyl-cyclobutanecarboxylic acid tert-butyl ester (step 2) (1.47 g, 7.38 mmol) in DCM (40 ml) was treated with TEA (2.57 ml, 18.44 mmol) followed by methyl 3-(chlorosulfonyl)benzoate (1.91 g, 8.11 mmol) and DMAP (0.09 g, 0.74 mmol). The mixture was stirred at RT for 2 h and then partitioned between DCM and water. The aqueous portion was extracted with DCM and the combined organic extracts were washed with 0.1N HCl, brine, dried over MgSO4 and concentrated in vacuo. Purification of the resulting oil by chromatography on silica eluting with 0-40% EtOAc in iso-hexane afforded the title compound as a colourless oil; 1H NMR (400 MHz, CDCl3) δ 8.56 (1H, s), 8.27 (1H, d), 8.08 (1H, d), 7.64 (1H, t), 5.21 (1H, br t), 3.98 (3H, s), 3.20 (2H, d), 2.37 (2H, m), 1.96 (4H, m), 1.46 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372845B2
Source datasetuspto-grants-2013_02
ORD IDord-e8c18e980a8440dd91d4abaf57117a64
Source noteuspto-grants-2013_02