HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726531Generated: November 2, 2026
Carbon tetrabromide → HCID 69041083, compound
https://huagongshe.com/reaction/1726531
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 69036644 | HCID 69036644 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69041083 | HCID 69041083 | 78% |
Reaction Steps
2.39 g (3.08 mmol) of 3,5-bis[(8-{2-methoxy-4-[(1E)-3-methoxy-3-oxo-1-propenyl]phenoxy}octyl)oxy]benzyl alcohol, 1,14 g (3.42 mmol) tetrabromomethane were dissolved in 25 ml dichloromethane. The solution was subsequently cooled to 0° C. and a solution of 0.86 g (3.29 mmol) triphenylphosphine in 20 ml dichloromethane was added dropwise thereto over a period of 1 hour. The mixture was subsequently allowed to react for 20 h at 25° C. and reduced in volume by evaporation. Chromatography of the residue on 120 g silica gel using first toluene:ethyl acetate (19:1) then (4:1) as eluant yielded 1.94 g (78%) 3,5-bis[(8-{2-methoxy-4-[(1E)-3-methoxy-3-oxo-1-propenyl]phenoxy}octyl)oxy]benzyl bromide as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07491752B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-2a725ff3b0914ee0a1db8b3dbc50bcf8 |
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| Source note | uspto-grants-2009_02 |
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