HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209463Generated: October 30, 2026
Trimethyl borate → (3-Chlorophenyl)boronic acid
https://huagongshe.com/reaction/2209463
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | HCID 21749248 | HCID 21749248 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3-Chlorophenyl)boronic acid | HCID 2734323 | — |
Reaction Steps
A solution of trimethylborate in 200 mL of ethyl acetate was cooled to -65° C. 3-Chlorobenzene magnesium chloride (0.8M, 60 mL), i.e., a grignard reagent, was added to the solution in a dropwise manner over 20 minutes. The mixture was kept in the temperature range of -60° C. to -70° C. and stirred. After 30 minutes, the mixture was allowed to warm to 0° C. and stirred for 1 hour. The mixture was quenched with H2O (25 mL) and stirred at room temperature for 1 hour. The solvent was removed and the remaining mass was extracted ethyl ether (3×100 mL). The organic layers were combined and washed with H2O (2×50 mL), dilute HCl (2×100 mL), H2O (2×50 mL) and brine (1×50 mL). The organic layer was dried with MgSO4, concentrated and allowed to stand. 100 mL of hexanes was added and the solution was stirred for 1 hour. The solution was filtered and allowed to air dry yielding 4.6 g of 3-chlorobenzene boronic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455252 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-d9ae3bb05887444f96e25c632c39d472 |
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| Source note | uspto-grants-1995_10 |
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