HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023820Generated: October 25, 2026
Potassium Carbonate → Tert-butyl(trans)-2-(3'-chlorobiphenyl-4-yl)cyclopropylcarbamate
https://huagongshe.com/reaction/1023820
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Chlorophenyl)boronic acid | HCID 2734323 | — |
| Reactant | tert-butyl ((1R,2S)-2-(4-bromophenyl)cyclopropyl)carbamate | HCID 86658779 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | Tert-butyl(trans)-2-(3'-chlorobiphenyl-4-yl)cyclopropylcarbamate | HCID 86680872 | 91% |
Reaction Steps
A solution of tert-butyl (trans)-2-(4-bromophenyl)cyclopropylcarbamate (Intermediate H, 3 g, 9.6 mmol), 3-chlorophenylboronic acid (1.8 g, 11.5 mmol) and K2CO3 (3.9 g, 28.8 mmol) in acetonitrile:water (4:1) was degassed for 20 min. Tetrakis triphenylphosphine palladium (300 mg) was added and heated at reflux for 18 h. After completion, the reaction mixture was poured into ice water (100 mL) and extracted with EtOAc (2×50 mL). The combined organic extracts were washed with water (50 mL), brine (50 mL) and dried over anhydrous Na2SO4 filtered and evaporated. The crude residue was purified by column chromatography (SiO2) using EtOAc: Pet ether to give (3 g, 91%) tert-butyl (trans)-2-(3′-chlorobiphenyl-4-yl)cyclopropylcarbamate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08722743B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-fe25649eba4b429a8a8fca3560739bf3 |
|---|
| Source note | uspto-grants-2014_05 |
|---|