Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582123Generated: November 1, 2026

Toluene → rac-tert-butyl N-[(1R,2S)-2-ethenylcyclopropyl]carbamate

https://huagongshe.com/reaction/582123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
SolventDiethyl EtherHCID 3283—
Productrac-tert-butyl N-[(1R,2S)-2-ethenylcyclopropyl]carbamateHCID 54277191—

Reaction Steps

The above acid (8.66 g, 77.43 mmol) was dissolved in anhydrous toluene (40 ml), cooled to 0°, treated with dry triethylamine (11.9 ml) and then, dropwise, with diphenylphosphoryl azide (23.4 g, Aldrich) in toluene (25 ml). The solution was warmed to 80° and kept at 80-85° for 45 mins. Anhydrous t-butanol (36 ml) and toluene (10 ml) were added quickly and the solution heated at 102° for 6 hours. The reaction mixture was allowed to cool and diluted with diethyl ether, washed with 1N orthophosphoric acid (100 ml), saturated aq.sodium bicarbonate and brine, dried and concentrated. The residual oil was purified by chromatography (silica: 350 g; hexane: ethyl acetate 95:5) to give the product as a colourless oil (3.91 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922748
Source datasetuspto-grants-1999_07
ORD IDord-519bc35b4be242dd899280b2ad3ac313
Source noteuspto-grants-1999_07