HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289407Generated: October 31, 2026
Carbon tetrabromide → 2,2-Bis(6-benzyloxyhexyl)ethyl bromide
https://huagongshe.com/reaction/1289407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,2-Bis(6-benzyloxyhexyl)ethanol | HCID 18920862 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Bis(6-benzyloxyhexyl)ethyl bromide | HCID 18920833 | 69.5% |
Reaction Steps
First, 13.8 g of 2,2-bis(6-benzyloxyhexyl)ethanol, 10.2 g of triphenylphosphine, and 50 ml of methylene chloride were placed in a 200 ml flask. Then, 50 ml of a methylene chloride solution containing 16.1 g of carbon tetrabromide was added dropwise to the reaction mixture at room temperature, and the reaction mixture was stirred for 1 hour. The reaction mixture was washed with an aqueous solution of sodium bicarbonate and water in this order. The resultant reaction mixture was dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: toluene) to obtain 11 g of 2,2-bis(6-benzyloxyhexyl)ethyl bromide (Y: 69%). The compound thus obtained had a purity of 97.5% by GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750213 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-e2cc117c2d364309b77d4aba6c91ee0c |
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| Source note | uspto-grants-1998_05 |
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