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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223319Generated: October 26, 2026

Water → N-Boc-1-fluoropent-4-EN-2-amine

https://huagongshe.com/reaction/223319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
Reactant1-Fluoropent-4-EN-2-amine hclHCID 20508329—
SolventTetrahydrofuranHCID 8028—
ProductN-Boc-1-fluoropent-4-EN-2-amineHCID 2050833785%

Reaction Steps

Tert-Butoxycarbonyloxyimino-2-phenylacetonitrile (3.34 g, 13.6 mmoles) in dry tetrahydrofuran (40 ml) is slowly added with ice cooling to a stirred mixture of 1-fluoro-2-amino-4pentene hydrochloride (1.9 g, 13.6 mmoles) prepared in Example 2 and triethylamine (2.78 g, 27.2 mmoles) in tetrahydrofuran (30 ml). After standing overnight (about 16 hours) at room temperature, water is added, the tetrahydrofuran is removed under reduced pressure, and the residue is extracted twice with ether. After washing with 1 N sodium hydroxide, then with water until neutral, the organic layer is dried and concentrated at reduced pressure to give 1-fluoro-2-tert-butoxycarbonylamino-4-pentene (2.33 g, 85%) as an oil which is used in Example 4 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04353828
Source datasetuspto-grants-1982_10
ORD IDord-19fabd3244a94c2db74dc639067bb9fb
Source noteuspto-grants-1982_10