HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532725Generated: October 26, 2026
Water → (Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylate
https://huagongshe.com/reaction/532725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | 4-Chloro-3-Fluorobenzaldehyde | HCID 2724985 | — |
| Reactant | Methyl2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetate | HCID 86599651 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylate | HCID 66617950 | 71.1% |
Reaction Steps
1,1,3,3-Tetramethylguanidine (2.11 ml, 16.8 mmol) was added to a 0° C. solution of methyl 2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)-acetate (5.00 g, 16.8 mmol) in DCM (70 mL). The reaction mixture was stirred at 0° C. for 30 minutes. Then a solution of 4-chloro-3-fluorobenzaldehyde (2.67 g, 16.8 mmol) in DCM (10 mL) was added by syringe. The reaction mixture was stirred for 10 minutes, then warmed to room temperature and stirred for another 1 hour. H2O was then added, and the mixture was extracted with DCM. The combined extracts were dried (Na2SO4), filtered, and concentrated. The resulting solids were recrystallized from IPA to give (Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylate (3.76 g, 67.8% yield) as a white powder (2 crops). LCMS (APCI−) m/z 328 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08853199B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-30ebf75709f443d0bfb2518cd29498f0 |
|---|
| Source note | uspto-grants-2014_10 |
|---|