HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367494Generated: October 29, 2026
Diethyl Ether → tert-Butyl 3-oxocyclopentane-1-carboxylate
https://huagongshe.com/reaction/1367494
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 3-Oxocyclopentanecarboxylic acid | HCID 227798 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 3-oxocyclopentane-1-carboxylate | HCID 14009986 | 96% |
Reaction Steps
To a cold (ice bath) solution of 3-oxo-1-cyclopentanecarboxylic acid (1.50 g), tert-butylalcohol (1.05 g) and 4-dimethylaminopyridine (140 mg) in dichloromethane (9 mL) was added a solution of dicyclocarbodiimide in dichloromethane (9 mL). The mixture was stirred 3 hours at ca. 2° C. then diethylether (30 mL) was added and the precipitate was filtered off and discarded. The solution was concentrated in vacuo. The residue was purified by flash chromatography on silica gel with cyclohexane/ethyl acetate (9:1 v/v) as eluant to afford the title compound (1.80 g, 96%) as colorless oil. MS (EI): 111 (M-OtBu.)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893099B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-cd421189375b431ca283a94321e025c6 |
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| Source note | uspto-grants-2011_02 |
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