HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227884Generated: October 31, 2026
Bis(4-chlorophenyl)acetic acid → HCID 18475024, compound
https://huagongshe.com/reaction/2227884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bis(4-chlorophenyl)acetic acid | HCID 6730 | — |
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18475024 | HCID 18475024 | 86.4% |
Reaction Steps
A suspension of the bis(4-chlorophenyl)acetic acid (10.40 g, 36.99 mmol) in dichloromethane (100 ml) was treated with oxalyl chloride (6.2 ml, 71.07 mmol) and dimethylformamide (1 drop). The mixture was stirred at room temperature overnight and was then concentrated under vacuum and coevaporated with toluene. The residue was dissolved in tetrahydrofuran (50 ml) and this solution was added to a mixture of 2-(methylamino)ethanol (6.0 ml, 74.7 mmol) in tetrahydrofuran (100 ml), water (50 ml) and sodium bicarbonate (10 g). The reaction was stirred at room temperature for 1 hour, then diluted with ethyl acetate. This was washed with water, HCl 1N, saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The residual white solid was crystallized from ethyl acetate to give the title compound (10.81 g, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06414179B1 |
|---|
| Source dataset | uspto-grants-2002_07 |
|---|
| ORD ID | ord-26afb04e619f4cd6947fd33a9aa24ab9 |
|---|
| Source note | uspto-grants-2002_07 |
|---|