HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527487Generated: November 3, 2026
Water → (3-Chloro-2-fluoro-5-vinyl-benzyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1527487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Carbamic acid, N-[(5-bromo-3-chloro-2-fluorophenyl)methyl]-, 1,1-dimethylethyl ester | HCID 68283623 | — |
| Product | (3-Chloro-2-fluoro-5-vinyl-benzyl)-carbamic acid tert-butyl ester | HCID 68283690 | — |
Reaction Steps
To a solution of (5-bromo-3-chloro-2-fluoro-benzyl)-carbamic acid tert-butyl ester (6 g, 17.7 mmol) in DME (100 mL) was added Pd(Ph3)4 (1.0 g, 0.9 mmol) under argon atmosphere and the mixture was stirred for 30 min at ambient temperature. After addition of vinyl boronic anhydride pyridine complex (4.3 g, 17.7 mmol), water (25 mL) and K2CO3 (2.45 g, 17.7 mmol) the reaction was heated under reflux for 7 h. The reaction mixture was concentrated in vacuo to half of the volume, quenched by addition of saturated aqueous NaHCO3 and extracted with EtOAc. After drying (Na2SO4) the solvent was removed in vacuo and the residue was purified by flash column chromatography on silica gel (eluent: hexane/EtOAc 9:1 to 4:1) to afford the title compound as a colorless oil. 1H-NMR (500 MHz, DMSO): δ (ppm) 7.62 (d, 1H), 7.45 (m, 1H, —NH), 7.35 (d, 1H), 6.68 (dd, 1H), 5.82 (d, 1H), 5.32 (d, 1H), 4.18 (d, 2H), 1.39 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09085555B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-cfb27d4d86444e32856b9edc89b2532d |
|---|
| Source note | uspto-grants-2015_07 |
|---|