HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536593Generated: October 29, 2026
Dimethylformamide → (+/-)Tert-butyl 7-formyl-8-azaspiro[4.5]decane-8-carboxylate
https://huagongshe.com/reaction/536593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 58348963 | HCID 58348963 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (+/-)Tert-butyl 7-formyl-8-azaspiro[4.5]decane-8-carboxylate | HCID 86664866 | 59.7% |
Reaction Steps
tert-butyl 8-azaspiro[4.5]decane-8-carboxylate (Intermediate 71, 6 g, 25.07 mmol) dissolved in 150 ml of Et2O was cooled to −78° C., then N,N,N′,N′-tetramethyl ethylendiamine (9.08 ml, 60.16 mmol) and secBuLi 1.4M in hexane (42.95 ml, 60.16 mmol) were added. After 10 minutes at −60° C., the temperature was raised to −20° C. for 60 minutes, then the reaction was cooled to −78° C. and dimethylformamide (4.47 ml, 60.16 mmol, dissolved in 5 ml of Et2O) was added. After 30 minutes a saturated aqueous solution of NH4Cl (30 ml) was slowly added, then reaction was allowed to reach room temperature. Reaction was extracted with Et2O (3×100 ml), the organic solvent was dried (Na2SO4) and evaporated to obtain 4 g of the title compound as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859608B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-82da4e89ad1748b0af2a62cfae2c75d7 |
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| Source note | uspto-grants-2014_10 |
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