HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440368Generated: November 1, 2026
Chloroethane → 4-Methoxyphenyl phenyl(2,4,6-trimethylbenzoyl)phosphinate
https://huagongshe.com/reaction/1440368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroethane | HCID 6337 | — |
| Reactant | 2,4,6-Trimethylbenzoyl chloride | HCID 97038 | — |
| Reactant | HCID 18983531 | HCID 18983531 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Methoxyphenyl phenyl(2,4,6-trimethylbenzoyl)phosphinate | HCID 18983502 | 65% |
Reaction Steps
59.5 g (0.326 mol) of 2,4,6-trimethylbenzoyl chloride and 0.75 g of triethylamine were heated to 115° C. and 45 g (0.163 mol) of monoethyl mono-4-methoxyphenyl phenylphosphonite were added dropwise in one hour under a nitrogen atmosphere and with vigorous stirring. Ethyl chloride was given off as a gas and was condensed in a downstream cold trap. The mixture was then further stirred at 110° to 115° C. for 90 minutes. In total, at the end of the reaction, 9 g (88% of theory) of ethyl chloride were situated in the cold trap. The excess 2,4,6-trimethylbenzoyl chloride was then distilled off at 1 mbar and the residue was distilled with the aid of a thin-film evaporator (bath temperature: 260° C.; 0.4 mbar). 40 g were obtained. The yield was 65% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05498741 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-d90c133c02834fc3b9b52884046adf04 |
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| Source note | uspto-grants-1996_03 |
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