HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443608Generated: October 29, 2026
Hydrochloric Acid → HCID 23468260, compound
https://huagongshe.com/reaction/443608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | 4-(Chloromethyl)benzoyl chloride | HCID 70136 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 23468260 | HCID 23468260 | — |
Reaction Steps
This ester was prepared by Method C by placing 72.1 g (0.5 mole) of β-naphthol, suspended in 150 ml of benzene, and 0.5 ml of pyridine in the vessel, adding all at once, at room temperature, a solution of 95 g (0.5 mole) of p-chloromethylbenzoyl chloride in 80 ml of benzene, and refluxing this reaction mixture for 6 hours, while passing a weak current of nitrogen through the apparatus. The HCl cleavage began at about 40° C., and at an internal temperature of 50° C., a clear, homogeneous solution had formed. After the end of the reaction time the benzene was substantially removed by distillation. The residue crystallized to a grayish pink crystal mass, the yield of which was quantitative (147.5 g). The raw ester melted at 90°-96° C. It was recrystallized from 2.5 liters of isopropanol with the addition of decolorizing carbon, yielding colorless, pearly, shiny flakes of a melting point of 102°-103.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04260803 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-02564b19fa7e40dea8458cecb0569de8 |
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| Source note | uspto-grants-1981_04 |
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