HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745397Generated: October 30, 2026
Chloromethyl Methyl Ether → HCID 131725674, compound
https://huagongshe.com/reaction/1745397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | 4-Hydroxyphthalic acid | HCID 11881 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131725674 | HCID 131725674 | — |
Reaction Steps
To a solution of 4-hydroxyphthalic acid (0.45 g, 2.47 mmol) in anhydrous N,N-dimethylformamide (5 ml) under nitrogen was added chloromethyl methyl ether (1.13 ml, 14.8 mmol) and diisopropylethylamine (2.6 ml, 14.8 mmol). The reaction was stirred at ambient temperature for 18 hours and then concentrated in vacuo. The crude material was partitioned between ethyl acetate (50 ml) and water (15 ml). The layers were separated, the organic layer washed with water (3×10 ml), brine (2×10 ml), dried (Na2 SO4), filtered and the solvent evaporated in vacuo. The resulting oil was dissolved in ethanol (5 ml) and sodium hydroxide (0.12 g, 7.4 mmol) dissolved in water (1 ml) was added to the reaction. The solution was stirred at ambient temperature for 48 hours and then concentrated in vacuo affording 4-methoxymethoxy-phthalic acid di-sodium salt, which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019026B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-b5351e0811f44e0cb7ac19fbb88f3c71 |
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| Source note | uspto-grants-2006_03 |
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