HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293006Generated: October 30, 2026
2-Ethylhexyl glycidyl ether → HCID 136395941, compound
https://huagongshe.com/reaction/2293006
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Ethylhexyl glycidyl ether | HCID 17162 | — |
| Reactant | HCID 135845402 | HCID 135845402 | — |
| Catalyst | Phosphonium, ethyltriphenyl-, bromide (1:1) | HCID 73727 | — |
| Solvent | Mesitylene | HCID 7947 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 136395941 | HCID 136395941 | 81.9% |
Reaction Steps
A mixture of 39.5 g (0.095 mol) of 2-mesityl-4,6-bis(2,4-dihydroxyphenyl)-1,3,5-triazine (compound 1b), 40.7 g (0.2185 mol) of 2-ethylhexyl glycidyl ether (purity 98%) and 3.5 g (9.5 mmol) of ethyltriphenylphosphonium bromide (purity 97%) in 250 ml of mesitylene (purity 99%) is stirred at 140° C. under nitrogen for 16 hours. The clear solution is freed from solvent under reduced pressure. The crude product is dissolved in 200 ml of ethyl acetate and filtered through a 6.0 cm layer of silica gel 60 (230-400 mesh) of diameter 8.0 cm, with elution with 1000 ml of ethyl acetate. Removal of the solvent and drying for 2 hours at 100° C. and a pressure of 0.6 mmHg (80 Pa) give 61.3 g (yield 81.8%) of the title product (compound 7; Tg 54.4° C.) of the formula ##STR106## where R=CH2 --CH(OH)--CH2O--CH2 --CH(C2 H5)--CH2CH2CH2CH3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686233 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-af18eca515804f41ae0c641590a67a28 |
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| Source note | uspto-grants-1997_11 |
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