HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907741Generated: October 25, 2026
1,2-Dichloroethane → Tert-butyl 4-(3-oxopyrrolidin-1-yl)benzoate
https://huagongshe.com/reaction/1907741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Tert-butyl 4-(3-hydroxypyrrolidin-1-yl)benzoate | HCID 10084125 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(3-oxopyrrolidin-1-yl)benzoate | HCID 10015517 | 29% |
Reaction Steps
A mixture of alcohol 266 (2.75 g, 10.45 mmol), NMO (5.8 g, 49 mmol) and 4 Å molecular sieves (8.34 g) was suspended in dry DCM (100 mL) and dry 1,2-dichloroethane (100 mL), stirred at room temperature for 45 min, and then cooled to 0° C. for the addition of solid TPAP (0.36 g, 1.03 mmol). The reaction mixture was stirred at 0° C. for 30 min and then at room temperature for 5 h, filtered through Celite®/silica gel using 50% AcOEt in hexanes as an eluent, then concentrated. The residue was purified by flash chromatography (eluent: 30% to 50% AcOEt in hexane) to provide title compound 267 (0.78 g, 29% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598168B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-7669fc4976394115afbe12a321938740 |
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| Source note | uspto-grants-2013_12 |
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