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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110311Generated: October 26, 2026

Hydrochloric Acid → 1-(1,3-Benzodioxol-5-yl)cyclobutanecarboxylic Acid

https://huagongshe.com/reaction/2110311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(1,3-Benzodioxol-5-yl)cyclobutanecarbonitrileHCID 21902008—
SolventEthylene GlycolHCID 174—
Product1-(1,3-Benzodioxol-5-yl)cyclobutanecarboxylic AcidHCID 2190202365%

Reaction Conditions

Temperature180 °C

Reaction Steps

1-Benzo[1,3]dioxol-5-yl-cyclobutanecarbonitrile (1.2 g) was slurried in ethylene glycol (10 mL) in a pressure tube and a large excess of KOH (1 g) was added. The tube was sealed and heated at 180° C. for 24 hours, cooled, poured into 100 mL of water, acidified with 1N HCl, extracted with ether, and the ether extracts were concentrated in vacuo and chromatographed on silica gel with an ethyl acetate:hexane:acetic acid mixture to give the desired 1-benzo[1,3]dioxol-5-yl-cyclobutanecarboxylic acid (850 mg, 65%). Data for this acid: MS 220 (M); 1H NMR (300 MHz, CDCl3): δ 11.4-11.8 (br. s, 1H), 2.78-6.85 (m, 3H), 5.95 (s, 2H) 2.75-2.85 (m, 2H), 2.40-2.55 (m, 2H), 1.8-2.2 (m, 2H); 13C NMR (75 MHz, CDCl3): δ 182.9, 147.9, 146.7, 137.2, 119.8, 108.2, 107.5, 101.3, 52.2, 32.6, 16.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517892B2
Source datasetuspto-grants-2009_04
ORD IDord-9bb0dd377fb54f008d01181a297b0403
Source noteuspto-grants-2009_04