HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486044Generated: October 30, 2026
Diisopropylamine → HCID 19097404, compound
https://huagongshe.com/reaction/486044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 19097377 | HCID 19097377 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19097404 | HCID 19097404 | 97.5% |
Reaction Steps
To a solution of diisopropylamine (13.2 mL, 94 mmol) in THF (175 mL) at -60° C. under nitrogen was added n-BuLi (36.2 mL, 94 mmol, 2.6 M hexane). The mixture was stirred for 30 minutes, cooled to -78° C. and ethyl 3,4,8-trimethyl-2-(phenylmethyl)-2-azabicyclo[2.2.2]octane-6-carboxylate (26.8 g, 85 mmol) in THF (225 mL) was added. The mixture was stirred for 3 hours, then ethyl chloroformate (8.96 mL, 94 mmol) in THF (20 mL) was added dropwise. The mixture was stirred for 24 hours, quenched with saturated NH4Cl, and poured into water (1000 mL). The solution was extracted with ether (3×), and the organic layers were combined and dried over MgSO4. The ether layer was treated with charcoal and the solvent was removed in vacuo to afford 32.1 g (97%) of diethyl 3,4,8-trimethyl-2-(phenylmethyl)-2-azabicyclo-[ 2.2.2]octane-6.6-dicarboxylate as a golden oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05290789 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-9c00e971918e4fd89445b8403c8937b4 |
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| Source note | uspto-grants-1994_03 |
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