Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586086Generated: November 1, 2026

Ethanol → HCID 178440759, compound

https://huagongshe.com/reaction/1586086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-tert-ButylbenzaldehydeHCID 70324—
ReactantHCID 21217850HCID 21217850—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
ProductHCID 178440759HCID 178440759—

Reaction Conditions

Temperature25 °C

Reaction Steps

To 4-tert-butylbenzaldehyde (0.4000 g, 0.00247 mol) was added 3 mL of 40% NaHSO3 (aq). The mixture was stirred for 2 h at 25° C. 3,4-Diaminobenzamidine dihydrochloride (0.56 g, 0.0025 mol) and ethanol (8 mL) were added. The mixture was refluxed for 3 h. The reaction was then poured into water. The precipitate filtered and recrystallized from 2N HCl to afford 1H-benzimidzole-5-carboximidamide, 2-[4-(1,1-dimethylethyl)phenyl]- (400 mg, 44%) as a white solid: 1H NMR (DMSO-d6) δ9.47 (bs, 2 NH), 9.15 (bs, 2 NH), 8.30 (d, 2 arom-H, J=8 Hz), 8.21 (s, 1 arom-H), 7.88 (d, 1 arom-H, J=8 Hz), 7.73 (d, 1 arom-H, J=9 Hz), 7.68 (d, 2 arom-H, J=8 Hz), 1.35 (s, 9 tert-butyl-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05942532
Source datasetuspto-grants-1999_08
ORD IDord-26a54a565a9747b1a9a83b4a5c6fe192
Source noteuspto-grants-1999_08