HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506750Generated: October 30, 2026
Triethylamine → N-(benzyloxycarbonyl)-4-(mesyloxy)butylamine
https://huagongshe.com/reaction/1506750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzyl N-(4-hydroxybutyl)carbamate | HCID 3366758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(benzyloxycarbonyl)-4-(mesyloxy)butylamine | HCID 11141145 | 81.3% |
Reaction Steps
To a solution of benzyl 4-hydroxybutylcarbamate (1.1 g, 4.9 mmol) and triethylamine (1.7 mL, 9.8 mmol) in THF was added methanesulfonyl chloride (0.67 g, 5.9 mmol) at 0° C. The reaction was stirred at 20-25° C. for 6 hours and concentrated. The residue was partitioned between ethyl acetate and water. The phases were separated, and the organic layer was washed with hydrochloride solution (1 N), saturated sodium bicarbonate solution, and saline. The separated organic layer was dried and concentrated to give 4-(benzyloxycarbonylamino)butyl methanesulfonate (1.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221760B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-b20122d48fe34482a3c16ad8d8803456 |
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| Source note | uspto-grants-2015_12 |
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