HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416990Generated: November 4, 2026
Tetramethylammonium hydroxide → HCID 67593023, compound
https://huagongshe.com/reaction/1416990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetramethylammonium hydroxide | HCID 60966 | — |
| Reactant | 1,1,1-Tris(4-hydroxyphenyl)ethane | HCID 93118 | — |
| Reactant | 1,3-Dioxane, 2-(2-bromoethyl)- | HCID 520656 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67593023 | HCID 67593023 | — |
Reaction Steps
26.8 g of tris(4-hydroxyphenyl)ethane was dissolved in 180 ml of acetonitrile in a flask and added with 126 ml of tetramethylammonium hydroxide (25% aqueous solution) and then, with 39.4 ml of 2-(2-bromoethyl)-[1,3]-dioxane. The resulting solution was heated to 80° C. and stirred for 10 hours. The reactant mixture was diluted with 250 ml of ethyl acetate and washed with 300 ml of 5% aqueous sodium hydroxide solution and then, with 300 ml of saline. The organic layer was dried over magnesium sulfate, filtered and deprived of the solvent. The residue was crystallized in methanol, to give 46 g of 1,1,1-tris-[4-(2-[1,3]-dioxan-2-yl ethoxy)phenyl]ethane as a white powder (mp=101° C.), represented by the following formula. ##STR9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05916995 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-8fee1f901dec4e208a173268dfd50e1b |
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| Source note | uspto-grants-1999_06 |
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