HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604760Generated: October 30, 2026
tert-butyl N-(4-aminobutyl)carbamate → HCID 85975644, compound
https://huagongshe.com/reaction/604760
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 85975644 | HCID 85975644 | 68.1% |
Reaction Steps
To a solution of the BOC protected diamine 9 (2.10 g, 0.01 mol) in anhydrous acetonitrile (50 mL) was added potassium carbonate (5.14 g) and the suspension was stirred at RT for 10 minutes. A solution of 4-bromobutyronitrile (1.65 g, 0.01 mol) in acetonitrile (25 mL) was added and the resulting mixture stirred at 50° C. for 24 hours. TLC (1:10:89 NH4OH:MeOH:CHCl3) showed that the reaction was 95% complete. The mixture was filtered to remove most of the inorganic salts and the acetonitrile was removed in vacuo to give a solid/oily residue that was purified by flash column chromatography (1:5:94 NH4OH:MeOH:CHCl3) to yield the product 10 as a clear oil (1.74 g, 61%), Rf=0.5 (1:10:89 NH4OH:MeOH:CHCl3); 1H NMR (CDCl3) d 4.79 (br s, 1H, NHCO), 3.12 (q, 2H, CH2), 2.74 (t, 2H, CH2), 2.60 (t, 2H, CH2), 2.46 (t, 2H, CH2), 1.81 (quin, 2H, CH2) 1.57-1.37 (m, 13H, 2×CH2, 3×CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910363B1 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-316cb1aee89b402c84d11f5313472cc2 |
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| Source note | uspto-grants-2011_03 |
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