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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486044Generated: October 30, 2026

Diisopropylamine → HCID 19097404, compound

https://huagongshe.com/reaction/486044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 19097377HCID 19097377—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19097404HCID 1909740497.5%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290789
Source datasetuspto-grants-1994_03
ORD IDord-9c00e971918e4fd89445b8403c8937b4
Source noteuspto-grants-1994_03