HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039368Generated: November 1, 2026
Carbon tetrabromide → HCID 22913643, compound
https://huagongshe.com/reaction/2039368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68153618 | HCID 68153618 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22913643 | HCID 22913643 | 94.8% |
Reaction Steps
3-(4-Ethoxy-2,3-difluorophenyl)propanol (s21) (9.4 g) and triphenylphosphine (17.1 g) were dissolved in methylene chloride (100 ml). Carbon tetrabromide (17.3 g) in methylene chloride (100 ml) solution was slowly added dropwise to the solution at room temperature, and the mixture was stirred at room temperature for another 3 hours. The reaction mixture was treated with a saturated aqueous solution of sodium hydrogencarbonate, and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure to leave a residue, pale yellow solids. The residue was purified by column chromatography with heptane as an eluent and silica gel as a stationary phase powder to give 3-(4-ethoxy-2,3-difluorophenyl) bromopropane (s22) (11.5 g). The yield based on the compound (s21) was 94.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580146B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-51b01ec17c0b4dc783bf29ed20ed2e5f |
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| Source note | uspto-grants-2013_11 |
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