HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892154Generated: October 29, 2026
Resorcinol → (2-[3-Hydroxyphenoxymethyl]-6-methylphenoxy)acetonitrile
https://huagongshe.com/reaction/892154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Resorcinol | HCID 5054 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Cyanomethoxy-3-methylbenzyl bromide | HCID 22241489 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2-[3-Hydroxyphenoxymethyl]-6-methylphenoxy)acetonitrile | HCID 22241289 | — |
Reaction Steps
Heated (60° C.) a mixture of 2-cyanomethoxy-3-methylbenzyl bromide (10.2 g, 42.7 mmoles, example 24), resorcinol (18.8 g, 171 mmoles), and potassium carbonate (47.2 g, 342 mmoles) in acetonitrile (140 mL) for two hours. The reaction is diluted with ether and washed three times with distilled water, once with brine, and dried over MgSO4. The organic layer is isolated and concentrated, and the resulting residue is purified by column chromatography (silica, 5% EtOAc/CH2Cl2) to yield the title compound as a white crystalline solid. MS(EI) 269 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005440B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-b9fa7fc851564ba8bade906282d5fb02 |
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| Source note | uspto-grants-2006_02 |
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