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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683938Generated: November 3, 2026

Cyanogen Bromide → HCID 9995821, compound

https://huagongshe.com/reaction/1683938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant4-amino-2-deoxy-2,3-didehydro-N-acetylneuraminic acidHCID 445533—
ReactantSodium AcetateHCID 517045—
SolventMethanolHCID 887—
ProductHCID 9995821HCID 9995821106.6%

Reaction Steps

5-(Acetylamino)-4-amino-2,6-anhydro-3,4,5-trideoxy-D-glycero-D-galacto-non-2-enonic acid (3 g, 10.35 mmol) was suspended in methanol (37.5 ml) and sodium acetate (1.89 g, 23.1 mmol) was added, causing a "caking" of the suspension and making stirring difficult. To this at 21° C. with exclusion of moisture was added a solution of cyanogen bromide (1.14 g, 10.8 mmol) in methanol (150 ml), in a dropwise manner. Stirring gradually became easier, until a readily stirrable suspension was obtained. Addition was complete in 3.5 hr. The mixture was then stirred at 21° C. with exclusion of moisture for 44 hr. The small amount of remaining solid was filtered off and solvent evaporated in vacuo to an orange-brown foam. The foam was taken up in methanol (125 ml) and with rapid stirring at 21° C. was treated dropwise with propan-2-ol (130 ml). The precipitate was filtered off, washed with iPrOH:MeOH 3:2, and combined filtrate and washings evaporated to give the title compound as a pale yellow foam (3.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639786
Source datasetuspto-grants-1997_06
ORD IDord-1bd2d4b451024932bb3c36f34d0cd157
Source noteuspto-grants-1997_06