HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681446Generated: October 26, 2026
Acetic Anhydride → Dimethyl 4-hydroxy-3,5-di-tert-butylbenzylphosphonate
https://huagongshe.com/reaction/1681446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | Phenol, 4-[(dimethylamino)methyl]-2,6-bis(1,1-dimethylethyl)- | HCID 66609 | — |
| Product | Dimethyl 4-hydroxy-3,5-di-tert-butylbenzylphosphonate | HCID 3314790 | — |
Reaction Steps
A thermostatically controllable reactor is charged with 263 g (1 mol) of (4-hydroxy-3,5-di-tert-butylbenzyl)dimethylamine und 500 g of petroleum ether 100/140. With stirring and blanketing with inert gas, the reaction mixture is heated to 80° C. and 130 g (1.05 mol) of trimethyl phosphite are run into the clear solution. With cooling, 107 g (1.05 mol) of acetic anhydride are then added dropwise over 2 hours at 80° C., and stirring is continued for 2 hours at 80° C. The solvent is removed by distillation until the temperature is 115° C. The residual reaction solution is cooled to room temperature and stirred with 1 liter of water. The crystallised product is filtered with suction, washed with petroleum ether 100/140 and dried, giving 307 g (93% of theory) of almost colourless dimethyl 4-hydroxy-3,5-di-tert-butylbenzylphosphonate of m.p. 156°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05171873 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-3109bebf2d074e728eb6450d2eb6d02f |
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| Source note | uspto-grants-1992_12 |
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