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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601926Generated: October 31, 2026

Methanol → 6-p-Tolyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylic acid

https://huagongshe.com/reaction/601926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 6-p-tolyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylateHCID 59180248—
SolventTetrahydrofuranHCID 8028—
Product6-p-Tolyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylic acidHCID 5918008851%

Reaction Steps

The title compound was synthesized from ethyl 6-p-tolyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylate (0.1423 g, 0.56 mmol, 1 equiv) and sodium hydroxide (1.4 mL, 14 mmol, 10M, 25 equiv), according to General Procedure 7. A 4-5:1 mixture of methanol (MeOH) and THF (5-6 mL) was used. The resulting product was purified by preparative HPLC using the Chromeleon purification system. A 0.1% formic acid/1% acetonitrile mixture in water (aqueous phase) and methanol (no modifier added—organic phase) using a 50 mm Dynamax HPLC C-18 column at 28 mL/min (initial gradient of 40% methanol and increasing to 100% over 7 minutes) afforded the title compound (68.9 mg, 51%) with purity by HPLC of 97.9% (UV). LCMS m/e 240.2 (M−H). 1H NMR (400 MHz, METHANOL-d4) δ ppm 2.17-2.26 (m, 1H), 2.29 (s, 3H), 2.62 (ddd, J=14.43, 6.06, 5.84 Hz, 1H), 2.68-2.77 (m, 1H), 2.85-2.96 (m, J=8.63, 8.49, 8.49, 4.20 Hz, 1H), 4.21 (dd, J=8.47, 5.42 Hz, 1H), 6.66 (s, 1H), 6.94-7.03 (m, 2H), 7.09 (d, J=7.91 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902252B2
Source datasetuspto-grants-2011_03
ORD IDord-7b542b09c8f148e4b87c435273c1a3b1
Source noteuspto-grants-2011_03