HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86741123, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | Hexahydronaphthalene-1,3(2h,4h)-dione | HCID 12453943 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86741123 | HCID 86741123 | — |
Reaction Steps
A solution of 1.06 gm (6.38 nmole) of decalin-1,3-dione in 3 mL of dry ethanol was cooled in an ice bath and treated with 0.89 mL of (6.4 mmole) triethylamine followed by 1.128 gm (6.50 mmole) of p-toluenesulfonyl azide. The mixture was stirred in the ice bath for 4 hours, then concentrated in vacuo (less than 40° C.). The residue was dissolved in 45 mL of ether and the ether washed with a solution of 0.42 gm KOH in 30 mL of water, dried (Na2SO4), filtered, and concentrated to 1.22 gm of an orange oil. This was chromatographed on 40-micron silica giving 0.45 gm of trans-2-diazodecalin-1,3-dione, mp 81°-3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04624908 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-0c22d4064dea420f8342e19d1f1a3d5a |
| Source note | uspto-grants-1986_11 |