HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381242Generated: November 2, 2026
Ammonia → 4-Benzyloxy-5-methoxy-2-(4-methylbenzoyl)benzonitrile
https://huagongshe.com/reaction/2381242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | (5-Benzyloxy-2-bromo-4-methoxyphenyl)p-tolylmethanone | HCID 53629725 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Benzyloxy-5-methoxy-2-(4-methylbenzoyl)benzonitrile | HCID 58345550 | 112% |
Reaction Steps
A mixture of (5-benzyloxy-2-bromo-4-methoxyphenyl)-p-tolylmethanone (reference example 10-1) (1.11 g), copper(I)cyanide (967 mg) and 1-methyl-2-pyrrolidinone (2 mL) was irradiated with microwave to heat at 200° C. for 10 min while stirring. Water, a 28% ammonia in water and ethyl acetate were added. The separated organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was triturated with diethyl ether to give the title compound (1.08 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258162B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-8cc61f0707c54dd58ee417a99f8df97d |
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| Source note | uspto-grants-2012_09 |
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