HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891920Generated: October 28, 2026
Dibromomethane → 2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
https://huagongshe.com/reaction/1891920
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Pinacol | HCID 6425 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 10955110 | 68% |
Reaction Steps
To a mixture of triisopropyl borate (20 g, 110 mmol), dibromomethane (8.6 mL, 120 mmol), and tetrahydrofuran (150 mL) was added dropwise n-butyl lithium (2.6 M n-hexane solution, 39 mL, 100 mmol) over a period of 1.5 hours at −78° C., and then the reaction mixture was stirred for 1.5 hours at the same temperature. This mixture was then stirred for 2 hours at room temperature, after which it was cooled to 0° C., methanesulfonic acid (6.5 mL, 100 mmol) was added to the reaction mixture, and then the reaction mixture was stirred for 1 hour at room temperature. The mixture was cooled to 0° C., pinacol (12 g, 100 mmol) was added to the reaction mixture, and the reaction mixture was then stirred for 1 hour at room temperature. The reaction mixture was concentrated under a reduced pressure, after which the residue thus obtained was distilled under a reduced pressure (74-76° C., 8 mmHg) to obtain the title compound (16 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507530B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-64907f955de0499aa92f068710010d7b |
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| Source note | uspto-grants-2013_08 |
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