Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Reactant | 2,6-Dichloro-4-hydroxybenzaldehyde | HCID 528382 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22322020 | HCID 22322020 | — |
Reaction Steps
82 mg (3.4 mmol) sodium hydride was added to an ice cooled solution of 500 mg (2.6 mmol) A1 and 342 mg (2.7 mmol) methoxyethoxymethylchloride in 5 ml dry dimethylformamide and the mixture was stirred at 60° C. for 8 hours. The solvent was distilled off and the residue was partitionated between aqueous ammonia and ethyl acetate. The organic layer was dried over sodium sulfate and evaporated to dryness yielding 370 mg (51%) A23, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790852B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-136f86cb57be4da1908b2b0185889327 |
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| Source note | uspto-grants-2004_09 |
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