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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061431Generated: November 2, 2026

Hydrochloric Acid → HCID 4186956, compound

https://huagongshe.com/reaction/2061431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-AminophenolHCID 11568—
ReactantPivaloyl chlorideHCID 62493—
SolventTolueneHCID 1140—
SolventSodium HydroxideHCID 14798—
ProductHCID 4186956HCID 4186956—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 3-amino-phenol (60 g, 6.55 mol) in 2 N NaOH (1 l), cooled to 10° C., pivaloyl chloride (68 ml, 0.55 mol) in toluene (200 ml) is added within 1 h. After stirring for 15 h at 25° C., the mixture is cooled to 0° C. and acidified to pH 1 with conc. HCl. Extraction with EtOAc washing with water, 10% NaHCO3, water, and brine, followed by drying (Na2SO4), evaporation of volatiles, and crystallization (EtOAc/hexanes) gives N-(3-hydroxy-phenyl)-2,2-dimethyl-propionamide. N-(3-Hydroxy-phenyl)-2,2-dimethyl-propionamide (49 g, 0.254 mol) in dichloromethane (1 l) is treated with dihydropyrane (66 ml, 0.762 mol) and pyridinium p-toluenesulfonate (957 mg, 3.8 mmol). After stirring for 6 days at 25° C., the solvent is removed and the residue crystallized from EtOAc/hexanes to give 2,2-dimethyl-N-[3-(tetrahydro-pyran-2-yloxy)-phenyl]-propionamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283356B2
Source datasetuspto-grants-2012_10
ORD IDord-1386570c9c1a4144802a120abba4f35a
Source noteuspto-grants-2012_10