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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398023Generated: November 2, 2026

Sodium Azide → Phenylmethyl 3-azido-4-hydroxy-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/1398023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantBenzyl 6-oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 22147363—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductPhenylmethyl 3-azido-4-hydroxy-1-pyrrolidinecarboxylateHCID 1969130565.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred mixture of benzyl 6-oxa-3-azabicyclo[3.1.0]hexane-3-carboxylate (5.2 g, 23.72 mmol) (Method 197) in DMF (30 mL) was added sodium azide (2.313 g, 35.58 mmol) in a mixture of acetone (20.00 mL) and water (10.00 mL). The resulting mixture was stirred at 80° C. for 24 h. The mixture was then diluted with water and ether, separated, and the organic layer was washed with brine, dried and conc. in vacuo. The resulting material was purified via silica gel chromatography (eluted with 15% to 35% ethyl acetate/hexane), yielding the title compound as a yellow solid (4.10 g, 65.9%). 1H NMR (400 MHz, dichloromethane-d2) δ ppm 7.50-7.25 (m, 5 H), 5.43-5.25 (m, 2 H), 4.31 (brs, 1 H), 4.00 (brs, 1 H), 3.77 (dd, 1 H), 3.69 (dd, 1 H), 3.53 (d, 1 H), 3.44 (dd, 1 H), 2.17 (brs, 1 H); m/z 263.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901307B2
Source datasetuspto-grants-2014_12
ORD IDord-a3e5487e861d4499b52363294d44328a
Source noteuspto-grants-2014_12