HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712203Generated: October 26, 2026
Triphenylphosphine → 5-Bromo-1,3-difluoro-2-[(octan-2-yl)oxy]benzene
https://huagongshe.com/reaction/1712203
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (+)-2-Octanol | HCID 2723888 | — |
| Reactant | 4-Bromo-2,6-difluorophenol | HCID 2736292 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-1,3-difluoro-2-[(octan-2-yl)oxy]benzene | HCID 68499982 | — |
Reaction Steps
12.0 g of 4-bromo-2,6-difluorophenol, 10.0 ml of (S)-(+)-2-octanol and 16.5 g of triphenylphosphine were dissolved in 300 ml of tetrahydrofuran at about 20° C. with stirring under a nitrogen atmosphere. 12.5 ml of anhydrous (max. 0.0075% of H2O) diisopropyl azodicarboxylate were subsequently added dropwise. The reaction proceeds exothermically. The rate of addition was selected in such a way that the temperature of the mixture did not exceed 45° C. The reaction solution was subsequently stirred for 2 h, and the solvent was then removed in a rotary evaporator. The crude product was purified in a mixture of chlorobutane and heptane in the ratio 1:1 over 2 l of silica gel, giving 14.5 g of 3,5-difluoro-4-(1-methylheptyloxy)bromobenzene as a clear liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790929B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-9693b3f43740458d867d347e8f2aae7b |
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| Source note | uspto-grants-2010_09 |
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