HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873828Generated: November 2, 2026
Tetrahydrofuran → 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1873828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | tert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate | HCID 11065582 | — |
| Reactant | HCID 178420676 | HCID 178420676 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester | HCID 10987983 | — |
Reaction Steps
To a 500 ml round bottom flask was added tert-butyl-4-{[methoxy(methyl)amino]carbonyl}piperidine-1-carboxylate (29 g, 106 mmol) and 150 ml tetrahydrofuran. The resulting solution was cooled with ice bath and methylmagnesium chloride tetrahydrofuran solution (42.6 ml, 3M, 128 mmol) was added by a syringe. The mixture was stirred at 0° C. for 30 minutes. It was diluted with 200 ml of ether and the resulting mixture was washed twice with 150 ml saturated ammonium chloride solution. The organics were dried over sodium sulfate, filtered and concentrated. The crude product was used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304434B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-cc4d041e11924b0daa6ad96abe7f9312 |
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| Source note | uspto-grants-2012_11 |
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