HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647136Generated: October 28, 2026
Bromomethyl 4-methoxyphenyl ketone → HCID 20485508, compound
https://huagongshe.com/reaction/647136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | HCID 12863631 | HCID 12863631 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20485508 | HCID 20485508 | — |
Reaction Steps
A suspension of 5-morpholino-1,2-dithiol-3-thione (2.62 g), 4-methoxyphenacyl bromide (4.12 g) and sodium iodide (3 g) in acetone (60 cc) is heated to the reflux temperature and maintained there for 2 hours. After cooling to a temperature of about 20° C., the insoluble product is filtered off and washed successively with acetone (30 cc), distilled water (2×40 cc) and acetone (2×30 cc). The product thus obtained is suspended in methylene chloride (110 cc). After stirring for 1 hour at a temperature of about 20° C., the insoluble product is separated by filtration. N-[5-(4-Methoxyphenacylthio)-1,2-dithiol-3-ylidene]-morpholinium iodide, melting at 152°-155° C., is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04407797 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-71e395ea46854b6b8a86782c7fe69491 |
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| Source note | uspto-grants-1983_10 |
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