HuagongsheHuagongshe Chemistry Print Report · For research reference only
Beta-Aminoisobutyric Acid → tert-butyl (6S)-6-formyl-5-azaspiro[2.4]heptane-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Beta-Aminoisobutyric Acid | HCID 64956 | — |
| Reactant | Tempo | HCID 2724126 | — |
| Reactant | (S)-Tert-butyl 6-(hydroxymethyl)-5-azaspiro[2.4]heptane-5-carboxylate | HCID 66848415 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl (6S)-6-formyl-5-azaspiro[2.4]heptane-5-carboxylate | HCID 71743236 | — |
Reaction Steps
To (S)-tert-butyl 6-(hydroxymethyl)-5-azaspiro[2.4]heptane-5-carboxylate (Intermediate 59, 2.2 g, 9.7 mmol) dissolved in 10 ml of DCM, TEMPO (306 mg, 1.9 mmol) and BAIB (3.43 mg, 10.6 mmol) were added. After 2 hours at 25° C., the reaction is diluted with DCM (150 ml), washed with an aqueous solution of Na2S2O3 then with water, dried (Na2SO4) and evaporated to obtain a crude that was purified by silica gel chromatography (petroleum ether to petroleum ether/ethylacetate 95/5). (S)-tert-butyl 6-formyl-5-azaspiro[2.4]heptane-5-carboxylate was obtained as light yellow solid (1.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859608B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-b2ae26e6f70c4220905d296676c2dadc |
| Source note | uspto-grants-2014_10 |