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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197443Generated: October 30, 2026

Acetic Anhydride → HCID 2742017, compound

https://huagongshe.com/reaction/2197443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86654171HCID 86654171—
SolventDichloromethaneHCID 6344—
ProductHCID 2742017HCID 274201798%

Reaction Steps

50 mg (1 eq.) of 4-(3-thiophen-2-yl[1,2,4]oxadiazol-5-yl)-piperidinium hydrochloride and 77 μl (3 eq.) of diisopropylethylamine were dissolved in 1 ml of dichloromethane. 39 μl (1.2 eq.) of acetic anhydride were added dropwise and the reaction medium was stirred for 2 hours at room temperature. The reaction medium was evaporated and the residue was taken up in 15 ml of ethyl acetate. The organic phase was washed with aqueous 1N sodium hydroxide solution (3×30 ml), with aqueous 1N hydrochloric acid solution (3×30 ml) and with saturated aqueous NaCl solution (30 ml), dried over MgSO4 and concentrated under reduced pressure to give 41 mg (98%) of the expected compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338599B2
Source datasetuspto-grants-2012_12
ORD IDord-936d5ea45c3744f2a2cbbd86ce4607bb
Source noteuspto-grants-2012_12