HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496775Generated: October 26, 2026
Sodium hydride → N-Boc-N-propyl-O-allylhydroxylamine
https://huagongshe.com/reaction/496775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | Carbamic acid, (2-propenyloxy)-, 1,1-dimethylethyl ester (9CI) | HCID 22322878 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Boc-N-propyl-O-allylhydroxylamine | HCID 22322817 | — |
Reaction Steps
N-Boc-O-allylhydroxylamine (6.5 g) from the above procedure was dissolved in dry THF (25 mL) and the solution cooled to 0° C. in an ice bath. Sodium hydride (1.5 g, 60% dispersion in oil) was added portionwise over 5 min. The resulting mixture was stirred for 30 min at 0° C. 1-Iodopropane (3.8 mL) was added dropwise to the mixture. The reaction was stirred at 0° C. for 1 hour, then stirred overnight at room temperature. The THF was removed in vacuo and the residue taken up in EtOAc (50 mL) and washed with water (1×50 mL), saturated sodium bicarbonate solution (3×50 mL), 1N phosphoric acid (3×50 mL), and brine (1×50 mL). The organic layer was dried with sodium sulfate and evaporated to give a light yellow oil, which was purified by flash chromatography on silica gel eluting with 5% EtOAc/hexanes to give the title compound as a colorless oil (6.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06946481B1 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-35d54636152b416396d59fd6ab5c7e3c |
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| Source note | uspto-grants-2005_09 |
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