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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988208Generated: November 4, 2026

Cyanogen Bromide → 2-(5-Amino-1,3,4-oxadiazol-2-yl)-1,1,1-trifluorobutan-2-ol

https://huagongshe.com/reaction/1988208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantButanoic acid, 2-hydroxy-2-(trifluoromethyl)-, hydrazideHCID 57729255—
SolventWaterHCID 962—
Product2-(5-Amino-1,3,4-oxadiazol-2-yl)-1,1,1-trifluorobutan-2-olHCID 46942198—

Reaction Steps

To hydrazide (34.07 g, 183 mmol) of step 2 in 275 mL of water was added KHCO3 (18.33 g, 183 mmol) followed by BrCN (19.39 g, 183 mmol) portionwise. After 3 h, the solid was filtered, washed with cold water and dried to afford the title compound. Additional compound could be recovered from the aqueous phase by extraction (ether-hexane, 1:1). 1H NMR (400 MHz, acetone-d6): δ 6.54 (s, 2H), 6.01 (s, 1H), 2.22 (m, 1H), 2.08 (m, 1H) and 0.99 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553973B2
Source datasetuspto-grants-2009_06
ORD IDord-b951095335714f0e81ea9d4706ed5ad4
Source noteuspto-grants-2009_06