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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740476Generated: November 1, 2026

Sodium Azide → HCID 57300086, compound

https://huagongshe.com/reaction/1740476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantHCID 54480540HCID 54480540—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57300086HCID 5730008692%

Reaction Conditions

Temperature80 °C

Reaction Steps

(2R,4R)-1-(tert-Butyloxycarbonyl)-2-(4,4'-Dimethoxytrityl)oxymethyl-4-[(p-toluenesulfonyl)oxy]pyrrolidine 39 (5.1 g, 7.58 mmol) was dissolved in dimethylformamide (50 ml) and diluted with water (5 ml ). To this stirred solution was added sodium azide (0.65 g, 10 mmol) and heated at 80° C. for 8 h. It was cooled and evaporated to dryness. The residue was partitioned between CH2Cl2 (200 ml) and water (100 ml), and extracted in CH2Cl2. The organic extract was washed with brine (50 ml), dried over Na2SO4 and evaporated to dryness. The crude product was purified by flash chromatography over silica gel using hexane→EtOAc as the eluent. The pure fractions were pooled together and evaporated to give 3.8 g (92%) of a clear oil. 1HNMR (CDCl3): 1.45 (s, 9H, Boc), 1.90 (dd, 1H), 2.34 (m, 1H), 3.40-3.62 (m, 3H), 3.74 (s, 6H, 2.0CH3), 4.00 (m, 2H), 4.28 (bs, 1H), 4.44 (m, 1H), 6.82 (d, 4H, Ph), and 7.26-7.80 (m, 9H, Ph).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05969135
Source datasetuspto-grants-1999_10
ORD IDord-18ca873b27a74843aa87c2882610be59
Source noteuspto-grants-1999_10