HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 21480268, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14346271 | HCID 14346271 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21480268 | HCID 21480268 | — |
Reaction Steps
12.72 g (18.2 mmol) of 2-[4-hydroxybenzyl)-1,4,7,10-tetrakis-(tert-butoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (example 9d) is dissolved in 250 ml of toluene and mixed with 350 mg of sodium hydride (80% in paraffin, 18.3 mmol). It is warmed to 80° to 100° C. and mixed by instillation with a solution of 1.74 g (18.2 mmol) of epichlorohydrin in 50 ml of toluene. After refluxing for two hours, it is concentrated by evaporation and purified over a silica gel column. A colorless oil is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05681543 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-ead090d7285c4b35aa99560bcae6b455 |
| Source note | uspto-grants-1997_10 |