HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894950Generated: October 25, 2026
Dichloromethane → 3-Phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate
https://huagongshe.com/reaction/894950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | — |
| Reactant | 2-(4-Chlorophenyl)-3-methylbutanamide | HCID 12898176 | — |
| Catalyst | Silver tetrafluoroborate | HCID 159722 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate | HCID 12898177 | — |
Reaction Steps
To a refluxing solution of 2.72 g (12.9 mmol) of 2-(4-chlorophenyl)-3-methylbutyramide and 2.27 g (8.6 mmol) of 3-phenoxybenzyl bromide in a solution of 15 ml dichloromethane and 3 ml ethyl ether is added a solution of 1.83 g (9.5 mmol) of silver tetrafluoroborate in ether. The mixture is refluxed for 2 hours and then separated by pouring into ice cold aqueous ethyl acetate/sodium bicarbonate. The organic phase is washed with water, dried and stripped of solvent. The residue is triturated with ether and filtered. The filtrate is concentrated and chromatographed on silica gel, eluting with 25% ethyl acetate/-hexane, and then on plates using 35% ethyl acetate/hexane, to yield 3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate, MS m/e 393 (M-hu +(M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04285879 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-63ef7c904ad547c69f6fe9cf27a5a4f1 |
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| Source note | uspto-grants-1981_08 |
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