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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073323Generated: November 1, 2026

Hydrochloric Acid → 9-Methyl(aminosulfonyl)fluorene-9-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1073323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantIodomethanesulfonamideHCID 519939—
ReactantEthyl 9H-fluorene-9-carboxylateHCID 596964—
ReactantBromomethanesulfonamideHCID 12268467—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product9-Methyl(aminosulfonyl)fluorene-9-carboxylic acid ethyl esterHCID 5411252431%

Reaction Steps

A mixture of fluorene-9-carboxylic acid ethyl ester (1) (11 g, 46.2 mmoL), potassium carbonate (6.4 g, 46.2 mmoL, 1 eq) and a mixture of bromomethanesulfonamide and iodomethanesulfonamide [prepared from bromomethanesulfonyl chloride see, Trice et al., J. Org. Chem., 32, 990(1967) by reaction with ammonia gas in cold ether followed by reaction with excess sodium iodide in refluxing acetonitrile] (9.1 g, 1 eq) in dry dimethylformamide (100 mL, from sieves) was stirred under nitrogen for 18 h. Water (200 mL) was then added and the solution was acidified with 1N aqueous hydrochloric acid (100 mL) and extracted with ethyl acetate (3×100 mL). The combined organic phases were then washed with brine (3×200 mL), dried (MgSO4), and concentrated. The residue was purified by column chromatography on silica gel using 40% ethyl acetate in hexane to provide 4.8g (31%) of product (2): mp 150°-156° C.; IR (KBr) 3360, 1710, 740, 725 cm-1 ; 1H NMR (CDCl3, 200 MHz) 7.78-7.69 (m, 4 H), 7.50-7.32 (m, 4 H), 4.38 (bs, 2 H, exchangeable), 4.12 (q. 2 H), 4.11 (s, 2 H), 1.12 (t, 3 H), MS m/z 331 (M+), 178 (base peak).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968809
Source datasetuspto-grants-1990_11
ORD IDord-4db2bbc8844f4c7a99fb728fcb231261
Source noteuspto-grants-1990_11