HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466340Generated: October 30, 2026
4,4,5,5-Tetramethyl[1,3,2]dioxaborolane → HCID 57764577, compound
https://huagongshe.com/reaction/1466340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,4,5,5-Tetramethyl[1,3,2]dioxaborolane | HCID 2734768 | — |
| Reactant | 4-[(4-Ethynylphenyl)methyl]morpholine | HCID 57764603 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57764577 | HCID 57764577 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999968B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-cdb76da82dfa4830a3dfcd213ea9e778 |
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| Source note | uspto-grants-2015_04 |
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