HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747748Generated: October 30, 2026
Triethylamine → benzyl (3R)-3-(4-cyanobenzoylamino)-4-(3-cyanophenoxy)butanoate
https://huagongshe.com/reaction/747748
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Cyanobenzoyl chloride | HCID 80172 | — |
| Reactant | benzyl (3R)-3-t-butoxycarbonylamino-4-(3-cyanophenoxy)butyrate | HCID 10960575 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | benzyl (3R)-3-(4-cyanobenzoylamino)-4-(3-cyanophenoxy)butanoate | HCID 11761964 | — |
Reaction Steps
1.8 g (4.38 mmol) of benzyl (3R)-3-t-butoxycarbonylamino-4-(3-cyanophenoxy)butanoate was dissolved in 20 ml of 4 N solution of hydrogen chloride in dioxane, and the solution was stirred at 0° C. for 6 hours. The solvent was evaporated, and the obtained oily residue was dissolved in 5 ml of dichloromethane. 1.09 g (6.58 mmol) of 4-cyanobenzoyl chloride and 1.22 ml (8.76 mmol) of triethylamine were added to the solution under cooling with ice, and they were stirred at room temperature overnight. The reaction mixture was treated with ethyl acetate as the extractant in an ordinary manner to obtain the crude product. After the silica gel column chromatography, the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396844B1 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-acf173b28bb543d1902de9ea09a112c9 |
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| Source note | uspto-grants-2008_07 |
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