HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28042Generated: October 29, 2026
Diethyl Ether → HCID 23338390, compound
https://huagongshe.com/reaction/28042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 23338371 | HCID 23338371 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23338390 | HCID 23338390 | — |
Reaction Steps
N-(4-Methyl-5-ethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline (0.25 mole), diethyl ether (30 ml), sodium carbonate (35.5 grams) and water (50 ml) are charged into a glass reaction vessel equipped with stirrer, thermometer and cooling means. The mixture is cooled to about 5° C. and chloroacetyl chloride (0.28 mole) is added dropwise with stirring. After the addition is completed, stirring is continued for 1 hour. After this time the organic phase is separated from the aqueous phase and is filtered. The filtrate is then washed with aqueous sodium carbonate, dried over anhydrous magnesium sulfate and filtered. The filtrate is then stripped of solvent under reduced pressure to yield the desired product N-(4-methyl-5-ethyl-1,3-dioxolan-2-ylmethyl)-2-methoxy-α-chloroacetanilide as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225335 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-62e7116f3bb5437b92717b29ff1160f3 |
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| Source note | uspto-grants-1980_09 |
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