HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488946Generated: October 29, 2026
Ethyl chloroformate → HCID 22268766, compound
https://huagongshe.com/reaction/488946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22268778 | HCID 22268778 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22268766 | HCID 22268766 | — |
Reaction Steps
Methyl 3-amino-5-(trifluoromethyl)benzoate (cf. procedures (116a) and (80a); 236 mg, 1.01 mmol) was dissolved in THF (11 mL) and the resulting solution was charged successively with K2CO3 (1.6 mL of a 2.0 M aq. solution) and ethylchloroformate (258 mg, 2.7 mmol). The reaction was stirred at RT for 48 h, concentrated in vacuo, and diluted with EtOAc. The organic phase was washed with sat. NaHCO3, water (2×), and brine before being dried (Na2SO4), filtered, and concentrated in vacuo. This product was dissolved in 3:1 THF/MeOH (8 mL) and the resultant solution was charged with lithium hydroxide (2 mL of a 1N solution). The reaction was stirred for 14 h, acidified with 1N HCl, and extracted with EtOAc (2×). The organic extracts were combined, washed with water, washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide 3-(ethoxycarbonyl)amino-5-(trifluoromethyl)benzoic acid. MS found: (M−H)−=276.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974836B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-3ef7f034819f42249018a6d26848780c |
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| Source note | uspto-grants-2005_12 |
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