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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662315Generated: October 30, 2026

Pentane → HCID 57705717, compound

https://huagongshe.com/reaction/1662315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantTrimethyl borateHCID 8470—
Reactant2-Bromo-1-butoxy-4-methoxybenzeneHCID 57801816—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57705717HCID 5770571731.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. solution of 2-bromo-1-butoxy-4-methoxybenzene 4.1 (250 mg, 965 μmol) in THF (8.0 mL) was added tert-butyllithium, 1.7 M solution in pentane (1248 μL, 2122 μmol) dropwise under a blanket of nitrogen. The pale yellow solution was stirred for 0.5 h at −78° C. before dropwise addition of neat trimethyl borate (175 μL, 1544 μmol) at the same temperature. The resulting mixture was stirred for 1 hour at −78° C., warmed to 25° C., and stirred for an additional hour. The reaction was quenched with saturated aqueous ammonium chloride and concentrated. The resulting residue was suspended in water/acetic acid (pH=3) and extracted with DCM. The combined organic layers were washed with saturated aqueous sodium bicarbonate and brine, dried (MgSO4), and concentrated to afford a light brown solid. The product was purified by trituration with hexane to afford 2-butoxy-5-methoxyphenylboronic acid 4.2 (67.2 mg, 31.1% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-4b9366b032df4e7da01a76f28b301963
Source noteuspto-grants-2011_10