Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899626Generated: November 2, 2026

Trimethyl borate → Boronic acid, (4-ethylphenyl)-

https://huagongshe.com/reaction/1899626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant1-Bromo-4-ethylbenzeneHCID 15313—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductBoronic acid, (4-ethylphenyl)-HCID 273435241%

Reaction Steps

A solution of 1-bromo-4-ethyl benzene (2.0 g, 11 mmol) in dry ether (5 ml) was added to magnesium turnings (311 mg, 13 mmol), which had been suspended in dry ether, by a dropwise addition. After addition was complete, the suspension was refluxed for a period of 15 min after which nearly all of the magnesium had reacted. This solution was then added to trimethy borate (1.12 g, 11 mmol) previously dissolved in ether (5 ml) at -78° C., the solution was warmed to room temperature and stirred for 90 min. The reaction was quenched by the addition of 10% aqueous HCl (2 ml) and the solution was extracted with ether. The combined ether extracts was extracted with 1M NaOH (2×20 ml), the aqueous extracts were acidified with dilute HCl to pH 2 and extracted with ether (2×25 ml). The combined ether extracts was washed once with water (10 ml), dried and evaporated to produce a white solid (676 mg, 38% yield), m.p. 138°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571821
Source datasetuspto-grants-1996_11
ORD IDord-9873f2f761ea4b78b2a2df31e89da22c
Source noteuspto-grants-1996_11