HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 3-[4-(2-Chloroacetylamino)-3-hydroxyphenyl]acrylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(4-Amino-3-hydroxyphenyl)-acrylic acid ethyl ester | HCID 54047397 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-[4-(2-Chloroacetylamino)-3-hydroxyphenyl]acrylic acid ethyl ester | HCID 54160237 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a stirred solution of 10-3 (3.38 g, 16.3 mmol) in CHCl3 (80 mL) was added saturated NaHCO3 (50 mL) and it was then chilled to 0° C. A solution of chloroacetyl chloride (1.94 mL, 24.4 mmol) in CHCl3 (30 mL) was added dropwise to the chilled biphase. Upon addition completion, the reaction was stirred at 0° C. for 1 h. The layers were separated and the aqueous layer was extracted twice with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4) and concentrated to give 10-4 which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06017926 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-a24781472ece49839d630c0d219d1c3d |
| Source note | uspto-grants-2000_01 |