HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → HCID 135740044, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Dibutyltin oxide | HCID 61221 | — |
| Reactant | HCID 135740159 | HCID 135740159 | — |
| Product | HCID 135740044 | HCID 135740044 | — |
Reaction Steps
A mixture of 3.00 g (4.00 mmol) of 2,4,6-tris(4-[1-ethoxycarbonyl-1-methylethoxy]-2-hydroxyphenyl)-1,3,5-triazine (Compound 1), 5.90 g (80.0 mmol) of n-butanol and 0.60 g (2.40 mmol) of dibutyltin oxide in 20 ml of xylene is heated at boiling for 16 h. The ethanol which forms is distilled off during the reaction. At the end of the reaction the solvent is distilled off in vacuo. The resultant residue is chromatographed on silica gel (Fluka, size 60 silica gel, 0.040-0.063 mm) with 5:1 hexane/diethyl ether. Following the removal of the solvent the product is obtained as a yellow oil which crystallizes on prolonged standing; m.p. 86-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06346619B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-a794a7ca05e94cd0a7a7bb8ea8f2bee6 |
| Source note | uspto-grants-2002_02 |