HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918331Generated: October 28, 2026
Hydrochloric Acid → 4-Borono-3-(2-m-tolyl-ethoxy)-benzoic Acid Methyl Ester
https://huagongshe.com/reaction/1918331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Bis(dimethylaminoethyl) ether | HCID 18204 | — |
| Reactant | 4-Iodo-3-(2-m-tolyl-ethoxy)-benzoic Acid Methyl Ester | HCID 67170900 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Borono-3-(2-m-tolyl-ethoxy)-benzoic Acid Methyl Ester | HCID 67169562 | 56.4% |
Reaction Steps
2.3 g of bis(2-dimethylaminoethyl)ether were dissolved in 50 ml of anhydrous THF and 7.1 ml of a 2 M solution of isopropylmagnesium chloride added at 15° C. The mixture was stirred for 20 min at 15° C. Then a solution of 4.7 g of 4-iodo-3-(2-m-tolyl-ethoxy)-benzoic acid methyl ester in 20 ml of anhydrous THF was added at room temperature. The mixture was stirred for 10 min at 20° C., and then 2.4 g of trimethyl borate were added dropwise at 0° C. and the mixture stirred for 20 min at 0° C. 100 ml of 0.1 N hydrochloric acid were added, and the mixture was extracted three times with 100 ml of EA. The combined organic layers were washed with 100 ml of water, dried with magnesium sulfate and evaporated. Silica gel chromatography (EA/HEP 1:5) of the residue yielded 2.1 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08618304B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-44b70de1b28444469d191317f0a809fd |
|---|
| Source note | uspto-grants-2013_12 |
|---|