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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004572Generated: October 26, 2026

Methane → HCID 178505406, compound

https://huagongshe.com/reaction/1004572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 10465169HCID 10465169—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178505406HCID 178505406—

Reaction Steps

The diamine (6.7 g, 0.035 mol) (obtained in step 4 above) was dissolved in ethanol (20 mL) and added to a stirred mixture of carbon disulfide (3.0 g, 0.04 mol), potassium hydroxide (2.3 g, 0.04 mol), water (5 mL) and ethanol (15 mL). The resultant solution was refluxed for 6 h. Animal charcoal (2.0 g) was added and further refluxed for 1 h. The mixture was filtered and washed with hot water. A mixture of acetic acid and water (1:2, 15 mL) was added to the filtrate slowly with vigorous stirring to separate 6-fluoro-5-(imidazol-1-yl)-2-mercapto-1H-benzimidazole (5.0 g, 60%) as a brown solid. mp 280° C. (decomp.); IR (KBr) 3078, 1481 cm-1 ; 1H NMR (DMSO-d6) δ 2.20 (s, 1H, SH), 7.10 (s, 1H), 7.24 (d, J=6.0 Hz, 1H), 7.26 (d, J=4.1 Hz, 1H), 7.56 (s, 1H), 8.00 (s, 1H), 12.90 (brs, 1H, NH); Mass (m/z) 234 (M+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051570
Source datasetuspto-grants-2000_04
ORD IDord-9cb100df7e064d638039fc754ff51fbe
Source noteuspto-grants-2000_04