HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → 2-Benzyl-5-carbethoxy-2,5-diazabicyclo[2.2.1]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-benzyl-5-(N,N-diethyl-carbamyl)2,5-diazabicyclo[2.2.1]heptane hydrochloride | HCID 21545496 | — |
| Reactant | 2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydroiodide | HCID 22403956 | — |
| Product | 2-Benzyl-5-carbethoxy-2,5-diazabicyclo[2.2.1]heptane | HCID 22099534 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947445 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-da63c3ee39cd40f5a28e404e0965ea10 |
| Source note | uspto-grants-1976_03 |