HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583474Generated: November 1, 2026
Pyridine → Methyl 3-chloro-4-methylcarbanilate
https://huagongshe.com/reaction/1583474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 3-Chloro-4-methylaniline | HCID 7255 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 3-chloro-4-methylcarbanilate | HCID 140888 | — |
Reaction Steps
To a stirred solution of 10.0 grams (0.071 mole) of 3-chloro-4-methylaniline in 100 ml of chloroform was added 16.7 grams (0.212 mole) of pyridine. Methyl chloroformate, 8.0 grams (0.085 mole), was then added dropwise during a 20 minute period. During the addition the reaction mixture temperature was held between 25°-30° C. with external cooling. Upon completion of addition the reaction mixture was stirred at ambient temperature for 16 hours. The reaction mixture was washed into a separatory funnel with 50 ml of chloroform; and the solution was washed with two 100 ml portions of water and 100 ml of aqueous 5% hydrochloric acid. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a waxy solid residue. The residue was recrystallized from hexane/ethyl acetate to give 10.9 grams of methyl(3-chloro-4-methylphenyl)carbamate; m.p. 80°-81.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04552585 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-f767c71a14fe4b4eb818c99a30ff4c5b |
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| Source note | uspto-grants-1985_11 |
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