HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242578Generated: October 28, 2026
m-Chloroperbenzoic acid → HCID 86597427, compound
https://huagongshe.com/reaction/242578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1,1-Dimethylethyl 4-(4-chlorophenyl)-3,6-dihydro-1(2H)-pyridinecarboxylate | HCID 15751425 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86597427 | HCID 86597427 | 71.5% |
Reaction Steps
To a cooled (0° C.) solution of 4-(4-chloro-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (7.10 g, approx. 24.1 mmol) in methylene chloride (150 mL) was added a solution of 3-chloroperbenzoic acid (75%, 8.34 g, 36.2 mmol) in methylene chloride (120 mL) over 40 min. The mixture was warmed to rt and allowed to stir over night (16 h). The solution was washed twice with a half-saturated aqueous solution of sodium bisfulfite to destroy excess oxidant. The mixture was then twice washed with half-saturated aqueous potassium carbonate, and brine. The extracts were dried over magnesium sulfate, filtered and concentrated to afford a crude oil which was purified by silica gel chromatography (100% hexanes-80% hexanes/20% ethyl acetate gradient) to afford pure 6-(4-Chloro-phenyl)-7-oxa-3-aza-bicyclo[4.1.0]heptane-3-carboxylic acid tert-butyl ester (5.34 g, 71%) as a clear, colorless oil which solidified on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08653096B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-9271a78e67244aa8bd3f9b84585058ee |
|---|
| Source note | uspto-grants-2014_02 |
|---|