HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006243Generated: October 26, 2026
Trimethyl borate → 4-(Cyclopropylmethoxy)phenylboronic acid
https://huagongshe.com/reaction/1006243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-(Cyclopropylmethoxy)-4-iodobenzene | HCID 22676731 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Cyclopropylmethoxy)phenylboronic acid | HCID 4198746 | — |
Reaction Steps
Butyl lithium (2.5 M in hexane, 14.4 mL, 36 mmol) was added dropwise (5 min) to a cooled (−78° C.) and stirred solution of 4-(cyclopropylmethoxy)iodobenzene 1 (9.00 g, 32.8 mmol) in tetrahydrofuran (100 mL). After 20 min, trimethyl borate (11.3 mL, 10.4 g, 100 mmol) was added dropwise (10 mL). The reaction was stirred for an additional 20 min, and was then allowed to warm to rt. The reaction was quenched with 1 M hydrochloric acid (300 mL) and stirring was continued for 30 min. The product was extracted with diethyl ether (4×100 mL) and then the combined organic extracts were dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was dissolved in toluene and then concentrated. This operation was repeated (5×) until the distillate was colorless and left 5.67 g (90%) of crude product. This material was used without purification or analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06787651B2 |
|---|
| Source dataset | uspto-grants-2004_09 |
|---|
| ORD ID | ord-50705a4d4be14f7091bc16391a203ded |
|---|
| Source note | uspto-grants-2004_09 |
|---|