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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602505Generated: November 2, 2026

2-Thiophenecarboxaldehyde, 5-chloro- → HCID 86607167, compound

https://huagongshe.com/reaction/602505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarboxaldehyde, 5-chloro-HCID 81700—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 28867605HCID 28867605—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 86607167HCID 8660716799%

Reaction Steps

A solution of N-(4-Amino-2-chlorophenyl)-2,2,2-trifluoroacetamide (4.567 g, 19.14 mmol) and 5-chloro-thiophene-2-carboxaldehyde (3.97 g, 27.1 mmol) in anhydrous ethanol (50 mL) was heated to reflux for 15 minutes and evaporated in vacuo at 70° C. (0.1 mbar, 30 min). The obtained crude imine as a crystalline solid was dissolved in methanol followed by addition of sodium cyanoborohydride (NaBH3CN) in methanol (50 mL) and acetic acid (9 mL) by portions. The obtained reaction mixture was stirred at room temperature for 60 minutes and evaporated in vacuo to small volume. The concentrated solution was quenched with water and filtered after 30 minutes to give 6.98 g (99% yield) of the title compound as a brown-yellow solid. 1H NMR (DMSO-d6): 4.43 (d, 2H), 6.63 (dd, 1H), 6.77 (d, 1H), 6.79 (t, 1H, NH), 6.94 (d, 1H), 6.97 (d, 1H), 7.10 (d, 1H), 10.85 (br. s, 1H, NHCO). LC/MS (m/z) 367.9 (M+); RT=3.36, (UV, ELSD) 99%, 100%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906537B2
Source datasetuspto-grants-2011_03
ORD IDord-618df8c13f8043d698bbf998b2f397d6
Source noteuspto-grants-2011_03