HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249282Generated: October 29, 2026
Triethylene Glycol → HCID 19825347, compound
https://huagongshe.com/reaction/2249282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylene Glycol | HCID 8172 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19825347 | HCID 19825347 | 90.7% |
Reaction Steps
To a solution of 355 mg (8.88 mmol) of sodium hydride contained at 60% in mineral oil in dry dimethylformamide (60 ml) was added 851 mg (5.67 mmol) of triethylene glycol in an atmosphere of argon, and the mixture was reacted at 40°-50° C. for 30 min. followed by addition of 3.37 g (13.5 mmol) of 4-bromobenzyl bromide. The mixture was allowed to react at room temperature for 18 hours. To the reaction mixture 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 dichloromethane yielded 2.51 g (5.14 mmol) of 1,12-bis(4-bromophenyl)-2,5,8,11-tetraoxadodecane.
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-0361b8e2fa0d4037af74549c22129c45 |
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| Source note | uspto-grants-1991_08 |
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