HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899676Generated: October 29, 2026
tert-butyl N-(4-aminobutyl)carbamate → HCID 69294992, compound
https://huagongshe.com/reaction/899676
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 117842630 | HCID 117842630 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69294992 | HCID 69294992 | 48.4% |
Reaction Steps
To a solution of 7-oxo-4,5,6,7-tetrahydorbenzoimidazole-1-carboxylic acid tert-butyl ester (632 mg, 2.82 mmol) in CH2Cl2 (50 mL) at room temperature under inert atmosphere was added (4-amino-butyl)carbamic acid tert-butyl ester (745 mg, 4.23 mmol) followed by sodium triacetoxyborohydride (896 mg, 4.23 mmol). The reaction mixture was stirred at room temperature for 17 hours. Saturated sodium bicarbonate solution (20 mL) was added and the mixture was extracted with dichloromethane (3×30 mL). The combined organic extracts were washed with brine, dried (MgSO4), filtered and concentrated. The resultant material was purified by column chromatography on silica gel (20:1:1 CH2Cl2:MeOH:NH4OH) to provide the product (558 mg, 48%): 1H NMR (CDCl3): δ 1.42 (s, 9H), 1.59 (s, 9H), 1.50-1.62 (m, 4H), 1.71-1.77 (2H), 1.82-2.00 (m, 2H), 2.06 (s, 1H), 2.73-2.87 (m, 4H), 3.09-3.13 (m, 2H), 3.33 (br s, 1H), 3.75-3.80 (m, 1H), 5.01 (br s, 1H), 7.96 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354932B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-2909e2f9ce0d488e9c78f42e341151c0 |
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| Source note | uspto-grants-2008_04 |
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