HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398258Generated: October 30, 2026
Sodium Chloride → HCID 23002572, compound
https://huagongshe.com/reaction/398258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86591389 | HCID 86591389 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23002572 | HCID 23002572 | 70% |
Reaction Steps
To a well-stirred reaction vessel equipped with a thermometer and a pH electrode were added 2-(4-methoxyphenoxy)acetyl 1-methyl-1-propyl carbonate (0.012 mole), 20 ml of diethyl ether, and 20 ml of a 25 wt % aqueous NaCl solution. The reaction mixture was cooled to below 10° C. and the pH was increased to a value above 11 using a 25 wt % aqueous NaOH solution. Then, TBHP (0.013 mole) was dosed with this temperature and pH being maintained. The mixture was post-reacted for 90 min at a temperature between 0 and 10° C. and a pH of above 11. Working up was as described in Example 1. After evaporation of the diethyl ether, 2.3 g of tert-butylperoxy 4-methoxyphenoxyacetate (an orange oil) having a content of 92.5% were obtained in a yield of 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610880B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-59ad5cc40a594ced8372291f7d4b6c32 |
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| Source note | uspto-grants-2003_08 |
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