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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177098Generated: October 26, 2026

Sodium Hydroxide → 4-[4-(Azetidine-1-carbonyl)-phenoxy]-2,2-dimethyl-2,3-dihydro-benzofuran-6-carboxylic acid

https://huagongshe.com/reaction/1177098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-[4-(Azetidine-1-carbonyl)-phenoxy]-2,2-dimethyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl esterHCID 59560251—
SolventMethanolHCID 887—
Product4-[4-(Azetidine-1-carbonyl)-phenoxy]-2,2-dimethyl-2,3-dihydro-benzofuran-6-carboxylic acidHCID 5955984677.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

Aqueous NaOH (3 N, 2.1 mL, 6.3 mmol) was added to a solution of 4-[4-(azetidine-1-carbonyl)-phenoxy]-2,2-dimethyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl ester (35b) (802 mg, 2.10 mmol) in 10 mL CH3OH. The mixture was heated to 60° C. for 3 hr, concentrated, diluted with H2O (60 mL) and acidified with 1N aqueous HCl to pH˜1. The aqueous phase was extracted with CH2Cl2 (60 mL), dried with MgSO4 and concentrated to give a white solid (598 mg, 74% yield). 1H NMR (400 MHz, DMSO-d6) δ 12.99 (s, 1 H) 7.67 (d, J=7.33 Hz, 2 H) 7.02-7.10 (m, 3 H) 6.99 (s, 1 H) 4.32 (s, 2 H) 4.03 (s, 2 H) 2.89 (s, 2 H) 2.21-2.30 (m, 2 H) 1.42 (s, 6 H); LCMS for C21H21NO5 m/z 468.00 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-4358c1da825445649a16e2c4b641dd13
Source noteuspto-grants-2010_11