HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263565Generated: October 31, 2026
Triisopropyl borate → 5-Allyl-2-hydroxy-3-methoxyphenylboronic acid
https://huagongshe.com/reaction/1263565
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 2H-Pyran, tetrahydro-2-(2-methoxy-4-(2-propen-1-yl)phenoxy)- | HCID 174886 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Allyl-2-hydroxy-3-methoxyphenylboronic acid | HCID 18616953 | 41% |
Reaction Steps
2-(4-Allyl-2-methoxyphenoxy)tetrahydropyran (2.0 g, 8.05 mmol) was dissolved in dry THF (70 ml) and the solution cooled to −78° C. sec-Butyl lithium (1.3M in hexanes, 7.4 ml, 9.62 mmol) was added dropwise with stirring over 10 minutes, the reaction was stirred at −78° C. for 2 hours. Triisopropoxy borane (3.4 ml, 14.6 mmol) was added and stirring continued for 4 hours at −78° C. The reaction was quenched with water, acidified to pH 1 with 2N hydrochloric acid and extracted with ether (2×200 ml). The combined extracts were dried with magnesium sulphate and concentrated under vacuum. The oily solid produced was triturated with cyclohexane and the solid filtered off to give the title compound (41%); MS 207 (M−H)−; HPLC retention time (system 1) 2.73 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06541490B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-a4856ba7822a4c26b6a5ce08bc558fe0 |
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| Source note | uspto-grants-2003_04 |
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