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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220494Generated: October 31, 2026

Sodium Azide → HCID 178476366, compound

https://huagongshe.com/reaction/2220494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178476345HCID 178476345—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventEthyl AcetateHCID 8857—
ProductHCID 178476366HCID 17847636675.3%

Reaction Steps

3,4,6-tri-O-Acetyl-2-deoxy-2-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-ethylamino]-α-D-glucopyranosyl bromide (3) (150 g, 0.282 mol) is suspended in ethyl acetate (3 L)and a solution of 10% aqueous sodium hydrogen carbonate (1500 mnL) containing sodium azide (22 g, 0.338 mol) is added. Tetrabutylammonium hydrogen sulfate (28.7 g, 30 mol %) was added and the biphasic mnixture stirred vigorously for 16 h. The organic layer was then separated, extracted and dried, then the solvent removed at reduced pressure. The residue was chromatographed as above to yield the desired product (105 g, 75%). 1H NMR (500 MHz, CDCl3) δ 13.90 (d, J=9.6, 1H), 5.22 (t, J=9.6, 1H), 5.11 (t, J=9.7, 1H), 4.90 (d, J=8.9, 1H), 4.36 (dd, J=4.5, 12.5, 1H), 4.17 (dd, J=12.4, 1.7, 1H), 3.81-3.91 (m, 2H), 2.60 (s, 3H, 2.42 (s, 2H), 2.36 (s, 2H), 2.11, (s, 3H), 2.04 (s, 3H), 1.03 (s, 3H). m/z 495 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417129B2
Source datasetuspto-grants-2008_08
ORD IDord-49774868ff294f679cb3a664549820c9
Source noteuspto-grants-2008_08