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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220282Generated: October 30, 2026

Acetic Anhydride → HCID 68415475, compound

https://huagongshe.com/reaction/220282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 68414384HCID 68414384—
ProductHCID 68415475HCID 68415475—

Reaction Steps

A solution of 3.66 g of [3-(4-amino-1H-benzoimidazol-2-yl)-propyl]-methyl-carbamic acid tert-butyl ester in 40 mL of acetic anhydride was refluxed for 2 h. The excess of acetic anhydride was evaporated off and the residue was treated with 16 mL of EtOH and IM-NaOH until pH 10 then extracted with EtOAc. The organic phase was dried over anh. Na2SO4 and concentrated in vacuo. Purification by CC using EtOAc/MeOH 100/1 to 90/1 yielded 1.86 g of [3-(4-acetylamino-1H-benzoimidazol-2-yl)-propyl]-methyl-carbamic acid tert-butyl ester as yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202885B2
Source datasetuspto-grants-2012_06
ORD IDord-0ae2e56943aa4ad9929c67571ab01696
Source noteuspto-grants-2012_06