HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430815Generated: October 30, 2026
4-tert-Butylbenzoic acid → N-[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-4-tert-butyl-benzamide
https://huagongshe.com/reaction/430815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylbenzoic acid | HCID 7403 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide | HCID 22255921 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-4-tert-butyl-benzamide | HCID 18352025 | — |
Reaction Steps
A solution of 0.589 g (3.026 mmol) 4-tert-butylbenzoic acid (Aldrich, Milwaukee Wis.) 1.06 mL (6.5 mmol) N,N-diisopropylethylamine, and 1.15 g (3.026 mmol) O-Benzotriazol-1-yl-N,N,N′,N′-bis(tetramethylene)-uronium hexafluorophosphate in 6 mL dry DMF was stirred in an ice bath for 35 minutes, when 1.00 g (3.026 mmol) of 2-Amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide (Example 1, Step B) was added. The resulting solution was warmed to 25° C. and stirred for 60 minutes. The mixture was poured into 20 mL diethyl and washed sequentially with 25 mL each of saturated aqueous sodium bicarbonate solution and twice with brine. The mixture was then dried over anhydrous sodium sulfate and concentrated at reduced pressure giving a pale amber solid that was purified by column chromatography on silica gel with 30% ethyl acetate in hexane to give N-[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-4-tert-butyl-benzamide as a white solid; mp 124-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323243B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-1f2627d0a6ee4a678b8bd880b3af32f6 |
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| Source note | uspto-grants-2001_11 |
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