HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628755Generated: October 29, 2026
Boron tribromide → Phenol, 4-((2-chloro-5-iodophenyl)methyl)-
https://huagongshe.com/reaction/628755
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 1-Chloro-4-iodo-2-(4-methoxybenzyl)benzene | HCID 86698896 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenol, 4-((2-chloro-5-iodophenyl)methyl)- | HCID 86698895 | 88.4% |
Reaction Steps
1-chloro-4-iodo-2-(4-methoxybenzyl)benzene (10.0 g, 27.9 mmol) was dissolved in methylene chloride (150 mL). To the resulting mixture was added dropwise boron tribromide (21 g, 83.7 mmol) under cooling in an ice-water bath. After the completion of dropwise addition, the mixture was warmed up to room temperature, and stirred for 3 hr. The mixture was quenched with a saturated sodium bicarbonate solution, was separated into an aqueous phase and an organic phase. The aqueous phase was extracted with methylene chloride (150 mL×2). The organic phases were combined, washed with a saturated sodium chloride solution, dried over anhydrous sodium sulphate, and concentrated under a reduced pressure. The resulting crude product was purified with a silica-gel column chromatography (ethyl acetate:petroleum ether=0-1:20) to produce 8.5 g of a product in a yield of 88%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315438B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-16f12484f6b9429b91f72350f4d9d671 |
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| Source note | uspto-grants-2016_04 |
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