HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920583Generated: October 29, 2026
Ammonium Chloride → Methyl 4-[4-[1-(2-ethoxy-2-oxoethyl)cyclopropyl]-2-(hydroxymethyl)butyl]benzoate
https://huagongshe.com/reaction/1920583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-[1-(2-Ethoxy-2-oxoethyl)cyclopropyl]-2-[4-(methoxycarbonyl)benzyl]butanoic acid | HCID 57965751 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-[4-[1-(2-ethoxy-2-oxoethyl)cyclopropyl]-2-(hydroxymethyl)butyl]benzoate | HCID 57965759 | — |
Reaction Steps
At −10° C., 12.31 ml of a 1 M borane/THF complex solution (12.31 mmol) are added dropwise to a solution of 2.23 g (6.15 mmol) of 4-[1-(2-ethoxy-2-oxoethyl)cyclopropyl]-2-[4-(methoxy-carbonyl)benzyl]butanoic acid in 50 ml of THF. After warming to 0° C., the mixture is stirred at this temperature for another 2 hours and then at room temperature for 1 hour. After complete conversion, saturated ammonium chloride solution is added, and the reaction mixture is extracted three times with in each case 50 ml of ethyl acetate. The combined organic phases are then dried over sodium sulfate, and the solvent is evaporated to dryness. The crude product obtained is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 2:1). This gives 1680 mg (78% of theory) of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08168821B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-9807b227d62f43279067a151cd96aa31 |
|---|
| Source note | uspto-grants-2012_05 |
|---|