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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778544Generated: November 3, 2026

Triethylamine → 7-Boc-9-Cbz-3-oxa-7,9-diazabicyclo[3.3.1]nonane

https://huagongshe.com/reaction/1778544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactanttert-Butyl 3-oxa-7,9-diazabicyclo(3.3.1)nonane-7-carboxylateHCID 53415349—
SolventDichloromethaneHCID 6344—
Product7-Boc-9-Cbz-3-oxa-7,9-diazabicyclo[3.3.1]nonaneHCID 11769810080%

Reaction Steps

To a solution of tert-butyl 3-oxa-7,9-diazabicyclo[3.3.1]nonane-7-carboxylate (0.500 g, 2.2 mmol) in dichloromethane (5 ml) was added triethylamine (0.443 g, 4.4 mmol) at room temperature. The mixture was stirred at room temperature for a few mins, and then benzyl chloroformate (0.751 g, 4.4 mmol) was added to the reaction mixture. The resulting mixture was stirred at room temperature overnight. The mixture was partitioned between dichloromethane and water. The organic phase was dried, and concentrated. The residue was purified by silica gel chromatography to give 9-benzyl 7-tert-butyl 3-oxa-7,9-diazabicyclo[3.3.1]nonane-7,9-dicarboxylate 133b (0.637 g, 80.0%). MS: calc'd (MH+) 363, measured (MH+) 363.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266904B2
Source datasetuspto-grants-2016_02
ORD IDord-f13193c56c164872b5c85dc6bc3ebf5e
Source noteuspto-grants-2016_02