HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541371Generated: October 30, 2026
Methyl chloroformate → 4-Cyclopropyl-2-ethyl-5-(methoxycarbonyl)benzoic acid
https://huagongshe.com/reaction/541371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 4-Cyclopropyl-2-ethyl-5-iodobenzoic acid | HCID 68288927 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Ether tetrahydrofuran | HCID 21868444 | — |
| Product | 4-Cyclopropyl-2-ethyl-5-(methoxycarbonyl)benzoic acid | HCID 68288152 | 102% |
Reaction Steps
To a solution of 4-cyclopropyl-2-ethyl-5-iodobenzoic acid (compound 226.5, 500 mg, 1.58 mmol, 1.00 equiv) in THF/Et2O (10/10 mL) under nitrogen at −78° C. was added dropwise n-butyllithium (2.5 M, 1.88 mL, 3.00 equiv) over 3 min. After stirring for 10 min at −78° C., methyl chloroformate (230 mg, 2.43 mmol, 1.50 equiv) was added dropwise at −78° C. The resulting solution was stirred for 40 min at −78° C., then warmed slowly to −35° C. The reaction was carefully quenched with 2 mL of water. The pH was adjusted to ˜4-5 with hydrogen chloride (aq., 1 M). The resulting mixture was extracted with 3×20 mL of ethyl acetate and the combined organic layers were dried (Na2SO4) and concentrated under reduced pressure to yield 400 mg the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08871790B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-747570201f1e4814bc98ef12ae9968ee |
|---|
| Source note | uspto-grants-2014_10 |
|---|