HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284871Generated: October 30, 2026
Dichloromethane → O2-benzyl O9-tert-butyl 2,9-diazaspiro[5.5]undecane-2,9-dicarboxylate
https://huagongshe.com/reaction/2284871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Tert-butyl 2,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride | HCID 71464197 | — |
| Solvent | Water | HCID 962 | — |
| Product | O2-benzyl O9-tert-butyl 2,9-diazaspiro[5.5]undecane-2,9-dicarboxylate | HCID 118049948 | 100% |
Reaction Steps
To a 20 L temperature controlled reactor charge tert-butyl 4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride (2.06 moles; 600.00 g) followed by dichloromethane (6.00 L), then triethylamine (4.33 moles; 604 mL) is added. Set the jacket of the reactor to 0° C. When the temperature of the reaction mixture reaches 5° C., add benzyl chloroformate (2.10 moles; 311 mL) over about 20 minutes keeping the internal temperature below 20° C. When the addition is complete, warm the jacket to room temperature and stir the mixture overnight. Pour the reaction mixture into water (4 L) and separate the mixture. Concentrate the organics under reduced pressure to give the title compound (838 g; assumed 95.65% purity and 100% yield for the purposes of calculation in the next reaction) mass spectrum (m/z): 411.2 (M+23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145437B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-9799e32c2a3048f4804da459b1d876e0 |
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| Source note | uspto-grants-2015_09 |
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