HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28040Generated: October 28, 2026
Diethyl Ether → N-(4-propyl-1,3-dioxolan-2-ylmethyl)-2-methoxy-alpha-chloroacetanilide
https://huagongshe.com/reaction/28040
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 23338370 | HCID 23338370 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-propyl-1,3-dioxolan-2-ylmethyl)-2-methoxy-alpha-chloroacetanilide | HCID 23338389 | — |
Reaction Steps
N-(4-Propyl-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-propyl-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-014ae2fa5ffd4701817a05d6204d0400 |
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| Source note | uspto-grants-1980_09 |
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