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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387153Generated: October 31, 2026

Hydrochloric Acid → 877133-14-7

https://huagongshe.com/reaction/2387153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 58764117HCID 58764117—
SolventWaterHCID 962—
Product877133-14-7HCID 5876421556.3%

Reaction Conditions

Temperature57.5 °C

Reaction Steps

Water (190 mL) was added to 5-(diethoxymethyl)-3-(difluoromethyl)-1-methyl-1H-1,2,4-triazole (47.6 g, 0.2024 mol, from Step 2), and the mixture was degassed. Then concentrated HCl (73 mL, 0.81 mol, 11.1 M) was added, and the mixture was stirred at 55-60° C. for 24 h. After this, the reaction mixture was evaporated, and the residue was repeatedly (8-10 times) evaporated with THF until the water and HCl were completely removed. The final residue was distilled under vacuum to give the crude title product (bp 46-50° C. at 0.04 mm Hg), containing, according to LC-MS data, 7% of a dimerization side-product. Further purification on a silica gel (ethyl acetate/hexane 1:3) yielded 18.37 g (56.3%) of 3-(difluoromethyl)-1-methyl-1H-1,2,4-triazole-5-carbaldehyde. Satisfactory C,H,N-analysis was obtained. 1H NMR (400 MHz, CDCl3): δ 4.25 (s, 3H), 6.74 (t, J=56 Hz, 1H), 10.01 (s, 1H). LC/MS (API-ES) calcd for C5H5F2N3O: 161.04, found (M+H+): 162.1; (M+18+H+): 180.1 m/z.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268835B2
Source datasetuspto-grants-2012_09
ORD IDord-c4185ae082214ca398aea50b5ac96d39
Source noteuspto-grants-2012_09