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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269129Generated: October 30, 2026

Hydrochloric Acid → (4-{[(3S)-3,7-Dimethyloct-6-en-1-yl]oxy}phenyl)boronic acid

https://huagongshe.com/reaction/1269129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant1-Bromo-4-{[(3S)-3,7-dimethyloct-6-en-1-yl]oxy}benzeneHCID 69380294—
SolventTetrahydrofuranHCID 8028—
Product(4-{[(3S)-3,7-Dimethyloct-6-en-1-yl]oxy}phenyl)boronic acidHCID 6937992467%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199167B2
Source datasetuspto-grants-2007_04
ORD IDord-aee2839c49784c98a72b1fd0d783e408
Source noteuspto-grants-2007_04