HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254374Generated: October 30, 2026
Triethylamine → {4-[4-(Carbamoylmethylamino)phenyl]butyl}carbamic acid tert-butyl ester
https://huagongshe.com/reaction/254374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromoacetamide | HCID 69632 | — |
| Reactant | [4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester | HCID 11558019 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {4-[4-(Carbamoylmethylamino)phenyl]butyl}carbamic acid tert-butyl ester | HCID 58664816 | 22% |
Reaction Steps
A mixture of [4-(4-aminophenyl)butyl]carbamic acid tert-butyl ester (0.8 g, 3.03 mmol), 2-bromoacetamide (0.46 g, 3.33 mmol), triethylamine (0.2 mL, 3.33 mmol), and DMF (30 mL) was stirred at 80° C. for 20 hours. TLC indicated that the reaction was not complete. Silver carbonate (0.92 g, 3.33 mmol) was thus added. The reaction was further stirred at 80° C. for 24 hours. The reaction mixture was passed through a silica plug. The solvent was evaporated in vacuo. The residue was purified by flash chromatography (silica gel, 3:1 ethyl acetate/dichloromethane, v/v) to provide 390 (0.20 g, 22%) as a white solid. 1H NMR (300 MHz, CD3OD) δ 1.42 (s, 9H), 1.55 (m, 4H), 2.50 (t, 2H), 3.03 (t, 2H), 3.70 (s, 2H), 6.52 (d, 211), 7.00 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875619B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-cb3e05fbd37642798c107f34bfedde25 |
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| Source note | uspto-grants-2011_01 |
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