HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645404Generated: October 29, 2026
Hydrochloric Acid → 2-(Chloromethyl)-3-methylnaphthalene-1,4-dione
https://huagongshe.com/reaction/1645404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Menadione | HCID 4055 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-(Chloromethyl)-3-methylnaphthalene-1,4-dione | HCID 123439 | 55% |
Reaction Steps
A mixture of 17.2 g (0.1 mole) of 2-methyl-1,4-napthoquinone and 6 g (0.2 mole) of paraformaldehyde was heated to 60° C. in 50 mL of glacial acetic acid and stirred while dry HCl was bubbled through the solution for about 3 hrs. To the cooled mixture was added 200 mL of water, the solid was filtered and rinsed with 50 mL of water. It was then suspended in 200 mL of CH2Cl2, filtered, rinsed with CH2Cl2, and the filtrate was water washed, dried, and evaporated to leave 20.5 g of crude 2-methyl-3-chloromethyl-1,4-napthoquinone. The crude product was purified by sublimation at about 100° C. and pressure of 0.05 mm to give 12.7 g. Since there had been some splatter during the sublimation, the product was resublimed to give 12.1 g (55% yield), m.p. 102-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124793B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-e7745c70daf94e29a47547374cda35e6 |
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| Source note | uspto-grants-2012_02 |
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