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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268231Generated: October 25, 2026

Ethyl chloroformate → 2-Benzyl-5-carbethoxy-2,5-diazabicyclo[2.2.1]heptane

https://huagongshe.com/reaction/268231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-benzyl-5-(N,N-diethyl-carbamyl)2,5-diazabicyclo[2.2.1]heptane hydrochlorideHCID 21545496—
Reactant2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydroiodideHCID 22403956—
Product2-Benzyl-5-carbethoxy-2,5-diazabicyclo[2.2.1]heptaneHCID 2209953468%

Reaction Steps

Using the procedure for preparation of 2-benzyl-5-(N,N-diethylcarbamyl)-2,5-diazabicyclo[2.2.1]heptane hydrochloride as related in Example 11, 29.0 g of 2-benzyl-2,5-diazabicyclo[2.2.1]heptane dihydroiodide, prepared according to the procedure given in Example 11, was treated with 1.5 equivalents of ethyl chloroformate to yield crude product. Dry column chromatography, a technique described by B. Loev and M. M. Goodman in Chem. Ind. (London), p 2026, 1967, on 1700 g alumina using chloroform development provided 11.6 g (68%) of pure product, characterized as the maleate salt, melting point 124°-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947445
Source datasetuspto-grants-1976_03
ORD IDord-da63c3ee39cd40f5a28e404e0965ea10
Source noteuspto-grants-1976_03