HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,3,5-Triiodo-2,4,6-tris-(oxiranylmethoxymethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3,5-Triiodo-2,4,6-trihydroxymethylbenzene | HCID 20693627 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Product | 1,3,5-Triiodo-2,4,6-tris-(oxiranylmethoxymethyl)benzene | HCID 18454879 | — |
Reaction Steps
55 ml of a 32% NaOH solution is added in drops at room temperature to a mixture that consists of 11.0 g (20.1 mmol) of 1,3,5-triiodo-2,4,6-trishydroxymethylbenzene, 55.5 g (0.6 mol) of epichlorohydrin and 1.1 g (3.2 mmol) of tetrabutylammonium hydrogen sulfate within 1 hour, and then it is stirred for 12 hours. It is mixed with 150 ml of water and extracted twice with 200 ml each of toluene. The combined organic phases are dried on sodium sulfate, the solvent is evaporated to the dry state and chromatographed on silica gel (mobile solvent:hexane/ethyl acetate 10:1). The fractions that contain the product are combined and concentrated by evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208140B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-b4c70f6b7b094d908dc42c6df188eb07 |
| Source note | uspto-grants-2007_04 |