HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463723Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 13560531, compound
https://huagongshe.com/reaction/463723
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-Chloromethyl-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methyl]isoquinoline | HCID 13560529 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13560531 | HCID 13560531 | 70.2% |
Reaction Steps
To an ice-cooled solution of 5.2 g 4-chloromethyl-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methyl]isoquinoline in 150 ml methylene chloride, was added under stirring and nitrogen a solution of 3.04 g m-chloroperbenzoic acid in 100 ml methylene chloride over 2 hours, so that the temperature did not exceed 3°-5°. The solution was stirred over night at room temperature and the red solution applied to a column, packed with 100 g silica gel 60 Merck, 230-400 mesh ASTM. From elution with ether and ethyl acetate the unreacted base 4-chloromethyl-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methyl]isoquinoline was separated. Elution with ethyl acetate/ethanol (4:1) afforded 3.8 g of a brownish foam. The 4-(chloromethyl)-1-(3,4-dimethoxybenzyl)-6,7-dimetoxyisoquinoline 2-oxide crystallized from methylene chloride/ethyl acetate: 3.5 g yellow crystals, mp 167°-168°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04544657 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-1e23e1c132554ae08333dbc8edf46b62 |
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| Source note | uspto-grants-1985_10 |
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