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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117334Generated: October 30, 2026

Hexane → 1-Benzothien-7-ylboronic acid

https://huagongshe.com/reaction/2117334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTrimethyl borateHCID 8470—
Reactant7-Bromobenzo[b]thiopheneHCID 12045538—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-Benzothien-7-ylboronic acidHCID 1664052860%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 7-bromo-1-benzothiophene (19.9 g, 0.094 mol) in absolute ether (200 ml) was treated with a 1.6 M solution of n-butyllithium in hexane (0.14 mol, 88 ml) at −78° C. The solution was stiffed at −78° C. for 10 minutes then treated with trimethyl borate (15 ml, 0.14 mol). The mixture was allowed to warm to −10° C. then quenched with an excess of dilute hydrochloric acid. The organic layer was separated, dried, evaporated, and the residue was recrystallised from aqueous ethanol to yield the title compound (10 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442701B2
Source datasetuspto-grants-2008_10
ORD IDord-ece564e6cbef422489e0a200676991f5
Source noteuspto-grants-2008_10