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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784795Generated: October 30, 2026

2,3-Dimethylphenol → HCID 68894799, compound

https://huagongshe.com/reaction/1784795

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DimethylphenolHCID 10687—
ReactantSodium HydroxideHCID 14798—
ReactantBenzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylateHCID 13186888—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68894799HCID 6889479951.4%

Reaction Steps

Benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (21.0 g, 92.0 mmol) was added to a stirred solution of 2,3-dimethylphenol (23.0 g, 188 mmol) and aqueous sodium hydroxide (100 ml, 2N, 200 mmol) in acetonitrile (400 ml). The reaction mixture was heated at reflux for 14 h. On cooling to room temperature, the reaction mixture was concentrated in vacuo before dilution with water (500 ml). Extraction with dichloromethane (4×100 ml) was followed by washing of the combined organics with aqueous sodium hydroxide (100 ml, 3N, 300 mmol), water (100 ml) and brine (100 ml). The organics were dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to furnish a crude product. Purification was carried out by silica gel chromatography using a gradient eluent system of iso-hexanes and ethyl acetate (100% iso-hexanes to 80:20 iso-hexanes:ethyl acetate) to furnish trans-benzyl-4-(2,3-dimethylphenoxy)-3-hydroxypiperidine-1-carboxylate as a pale yellow syrup (16.8 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504419B2
Source datasetuspto-grants-2009_03
ORD IDord-7baff472628c4fd88598f675370fa9fd
Source noteuspto-grants-2009_03