HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984143Generated: October 31, 2026
Hydrochloric Acid → (4-{[(3S)-3,7-Dimethyloct-6-en-1-yl]oxy}phenyl)boronic acid
https://huagongshe.com/reaction/984143
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-Bromo-4-{[(3S)-3,7-dimethyloct-6-en-1-yl]oxy}benzene | HCID 69380294 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-{[(3S)-3,7-Dimethyloct-6-en-1-yl]oxy}phenyl)boronic acid | HCID 69379924 | 67% |
Reaction Steps
2.5M n-Butylithium in hexanes (49.3 cm3, 0.12 mol) was added dropwise to a cooled (−78° C.) solution of 1-bromo-4-[(S)-3,7-dimethyloct-6-enyloxy]benzene (35 g, 0.11 mol) in tetrahydrofuran (350 cm3). The resultant solution was stirred at this temperature for 1 h and then trimethyl borate (23.8 g, 0.23 mol) was added dropwise to the mixture while maintaining the temperature at −78° C. 20% hydrochloric acid (250 cm3) was added and the resultant mixture was stirred for 1 h and then extracted into diethyl ether (2×200 cm3). The combined organic layers were washed with water (2×100 cm3) and dried (MgSO4). After filtration the solvent was removed under reduce pressure to yield 20.35 g (65%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06867243B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-fd84446e7ff94435a5664ed7c15900e6 |
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| Source note | uspto-grants-2005_03 |
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