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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720047Generated: October 26, 2026

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

https://huagongshe.com/reaction/720047

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 numberUS07132551B2
Source datasetuspto-grants-2006_11
ORD IDord-95aea27b3a2f4fd1aebd0e989a163585
Source noteuspto-grants-2006_11