HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421367Generated: October 30, 2026
Pyridine → Methyl 4-[(chlorocarbonyl)oxy]benzoate
https://huagongshe.com/reaction/1421367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Methylparaben | HCID 7456 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4-[(chlorocarbonyl)oxy]benzoate | HCID 854163 | — |
Reaction Steps
A 20% solution of phosgene (170 mL, 0.33 mol) in toluene was added to a 500 mL pear-shaped flask (flame-dried, N2). To the flask was added methyl-p-hydroxybenzoate (42.6 g, 0.28 mol) with stirring. Through an addition funnel was added pyridine (26.7 mL, 0.33 mol) in toluene while the reaction mixture was cooled in an ice bath so that the temperature did not exceed 20° C. The solution turned a yellowish color during the addition. The reaction mixture was stirred for 3 h, at which point the mixture was filtered on a buchner funnel. The pyridinium salts were washed with toluene (150 mL) and the combined organic phase washed with 1 N HCl (2×), water (2×), dried over CaCI2 and Na2SO4, and the toluene removed in vacuo to yield yellowish crystals. After continued drying, the product (38 g, 63%) turned a greyish color. m.p. 52-53° C. (lit. 51-52° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06075141 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-4306e441833c46abb49e6167519d5a8f |
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| Source note | uspto-grants-2000_06 |
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