HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273385Generated: October 25, 2026
Hydrochloric Acid → HCID 23157606, compound
https://huagongshe.com/reaction/273385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 2-Bromo-5-(2-ethoxyethoxy)-1,3-dimethylbenzene | HCID 23157690 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23157606 | HCID 23157606 | 68% |
Reaction Steps
To a solution of 2-bromo-5-(2-ethoxyethoxy)-1,3-dimethylbenzene (10.0 g, 36.6 mmol) in tetrahydrofuran (100 mL) was added n-butyllithium hexane solution (1.6 M, 25.1 mL, 40.2 mmol) at −78° C. with stirring. The reaction mixture was stirred at the same temperature for 30 min. and triisopropyl borate (10.5 mL, 45.5 mmol) was added. The reaction mixture was warmed to room temperature and stirred for 3 hrs. 5 N Hydrochloric acid (20 mL) was added to the reaction mixture and the mixture was partitioned between ethyl acetate and water. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was washed with hexane/diethyl ether and dried to give the title compound (5.9 g, yield 68%) as pale-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456218B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-ad9e6a63e53d436498e9e47182cf34ba |
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| Source note | uspto-grants-2008_11 |
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