Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383659Generated: November 2, 2026

4,4,5,5-Tetramethyl[1,3,2]dioxaborolane → HCID 57764577, compound

https://huagongshe.com/reaction/2383659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
Reactant4-[(4-Ethynylphenyl)methyl]morpholineHCID 57764603—
SolventTolueneHCID 1140—
ProductHCID 57764577HCID 5776457779%

Reaction Conditions

Temperature50 °C

Reaction Steps

An oven-dried round-bottom flask was cooled under N2 (g) and then charged with 4-(4-ethynylbenzyl)morpholine (120 mg, 0.596 mmol), toluene (2.5 mL), and 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.43 mL, 2.98 mmol). The mixture was stirred for 15 min while purging the solution with N2 (g). HRuCl(CO)(PPh3)3 (29 mg, 0.030 mmol) was then added and the reaction heated to 50° C. for 18 h. The reaction was quenched with NaHCO3 (sat.) (10 mL), extracted with EtOAc, and the organic layer washed with brine (2×) and then dried over MgSO4. The solvent was removed and the resulting residue purified by column chromatography (silica gel, Hexanes/EtOAc, 2:3 to 1:2) to give a white solid (155 mg, 79%). 1H NMR (400 MHz, CDCl3) δ 7.44 (d, 2H, J=8.0 Hz), 7.38 (d, 1H, J=18.8 Hz), 7.30 (m, 2H), 6.15 (d, 1H, J=18.5 Hz), 3.72 (bs, 4H), 3.49 (bs, 2H), 2.45 (bs, 4H), 1.31 (s, 12H); MS ESI 330.1 [M+H]+, calcd for [C19H28BNO3+H]+330.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263596B2
Source datasetuspto-grants-2012_09
ORD IDord-f8c7630fc7fd45b58acfe5858d50133f
Source noteuspto-grants-2012_09