HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784795Generated: October 30, 2026
2,3-Dimethylphenol → HCID 68894799, compound
https://huagongshe.com/reaction/1784795
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dimethylphenol | HCID 10687 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate | HCID 13186888 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 68894799 | HCID 68894799 | 51.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504419B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-7baff472628c4fd88598f675370fa9fd |
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| Source note | uspto-grants-2009_03 |
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