Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylene Glycol | HCID 8117 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromo-1-(bromomethyl)-2-chlorobenzene | HCID 21914486 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19825392 | HCID 19825392 | — |
Reaction Steps
To a solution of 472 mg (11.8 mmol) of sodium hydride contained at 60% in mineral oil in dry dimethylformamide (50 ml) was added 500 mg (4.71 mmol) of diethylene glycol in an atmosphere of argon, and the mixture was allowed to react at 40°-50° C. for 30 min. Then, 2.96 g (10.4 mmol) of 4-bromo-2-chlorobenzyl bromide was added, and the mixture was reacted at room temperature for 16 hours. To the reaction solution at 0° C. was added a saturated aqueous solution of ammonium chloride followed by extraction with ethyl acetate. The organic layer was washed with water and then concentrated under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography for separation and purification. Elution with ethyl acetatehexane (1:3) yielded 2.10 g (4.09 mmol) of 1,9-bis(4-bromo-2-chlorophenyl)-2,5,8-trioxanonane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05043142 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-72b1fce3b98f45a1a7edabb54c8c6fce |
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| Source note | uspto-grants-1991_08 |
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