Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908325Generated: October 27, 2026

Lithium hydroxide, monohydrate → 1-(2-Oxo-2,3-dihydro-1,3-benzoxazol-5-YL)cyclopropane-1-carboxylic acid

https://huagongshe.com/reaction/1908325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 1-(2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)cyclopropanecarboxylateHCID 59129179—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-(2-Oxo-2,3-dihydro-1,3-benzoxazol-5-YL)cyclopropane-1-carboxylic acidHCID 5912924784.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-(2-oxo-2,3-dihydro-benzooxazol-5-yl)-cyclopropanecarboxylic acid methyl ester (1.9 g, 8.1 mmol) in MeOH (20 mL) and water (2 mL) was added LiOH.H2O (1.7 g, 41 mmol) in portions at room temperature. The reaction mixture was stirred for 20 hours at 50° C. MeOH was removed by evaporation under vacuum before water (100 mL) and EtOAc (50 mL) were added. The aqueous layer was separated, acidified with HCl (3 mol/L) and extracted with EtOAc (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under vacuum to give 1-(2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)cyclopropanecarboxylic acid (1.5 g, 84%). 1H NMR (DMSO, 400 MHz) δ 12.32 (brs, 1H), 11.59 (brs, 1H), 7.16 (d, J=8.4 Hz, 1H), 7.00 (d, J=8.0 Hz, 1H), 1.44-1.41 (m, 2H), 1.13-1.10 (m, 2H). MS (ESI) m/e (M+H+) 218.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-0485aeed8779472bb91b2c0a4fa90c84
Source noteuspto-grants-2013_12