HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399191Generated: October 30, 2026
Hydrochloric Acid → 3-Benzyloxy-phenylboronic acid
https://huagongshe.com/reaction/2399191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-(Benzyloxy)-3-bromobenzene | HCID 2756638 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Benzyloxy-phenylboronic acid | HCID 2734313 | 62.5% |
Reaction Steps
62 g (0.236 mol) of 3-benzyloxybromobenzene, 6.64 g (0.277 mol) of magnesium and 0.3 g of iodine are reacted in 800 ml of tetrahydrofuran at 60° C. for 2 hours to give the solution of the corresponding Grignard compound, which is subsequently added dropwise to a solution, cooled to 0° C. of 28.77 g (0.277 mol) of trimethyl borate in 300 ml of tetrahydrofuran. The mixture is stirred at 0° C. for 1 hour, 74 ml of 37% strength hydrochloric acid in 300 ml of water are added, and the reaction mixture is subsequently partitioned between water and ether. The organic phase is washed twice with water, dried over sodium sulfate, evaporated and recrystallized from hexane, giving 33.65 g of 3-benzyloxybenzeneboronic acid. ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05447656 |
|---|
| Source dataset | uspto-grants-1995_09 |
|---|
| ORD ID | ord-74ddc87aa2504f00be47ec1fc3f5923b |
|---|
| Source note | uspto-grants-1995_09 |
|---|