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

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.

1. additionAfter addition
2. customhad reacted
3. customThe reaction was quenched by the addition of 10% aqueous HCl (2 ml)
4. extractionthe solution was extracted with ether
5. extractionThe combined ether extracts was extracted with 1M NaOH (2×20 ml)
6. extractionextracted with ether (2×25 ml)
7. washThe combined ether extracts was washed once with water (10 ml)
8. customdried
9. customevaporated

ORD record

ord-c1c147a2cbeb4858ba5715228f5b065a

Source dataset

uspto-grants-1997_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05591761