HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate → Tert-butyl (2S)-2-acetylpyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate | HCID 2734674 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Product | Tert-butyl (2S)-2-acetylpyrrolidine-1-carboxylate | HCID 10465808 | — |
Reaction Steps
25 ml (75 mmol) 3 M methylmagnesium chloride (diethyl ether) and 8.25 g (41.4 mmol) BOC-L-prolinal were allowed to react at −80° C. for 30 min according to procedure F. Yield of the crude product 9.19 g. The product was purified with a silica column using 33% ethyl acetate in petroleum ether as eluent. Yield 7.54 g (35.0 mmol 85%). The product was oxidized to the corresponding ketone according to procedure G. Yield of crude product 6.91 g. The product was purified with a silica column using 20–25% ethyl acetate in petroleum ether as eluent. Yield 5.61 g (26.3 mmol, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173024B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-201f7ab94c124c3b8eee44a569b0fb0c |
| Source note | uspto-grants-2007_02 |