Because of their unique properties and high biological activities, organophosphorus compounds have been used worldwide in agricultural, industrial, medicinal, and veterinary applications. Conventional strategies for direct phosphonylation suffer from the usage of stoichiometric or excessive metallic or nonmetallic catalysts and long reaction times under harsh conditions, leading to a strong desire for environment-friendly protocols for phosphonylation. A protocol for the accelerated phosphonylation of N-phenyltetrahydroisoquinolines in minutes was developed without the use of any catalyst in microdroplets. The phosphonylation process was completed (>85% yields) in 10 min at 40 °C using 0.8 equiv 2,3-dicyano-5,6-dichlorobenzoquinone as the oxidant and acetonitrile as the solvent. The microdroplet phosphonylation strategy showed good suitability to alkyl phosphites and N-phenyltetrahydroisoquinolines bearing electron-withdrawing and electron-donating substitutes, and the yields of the microdroplet reaction were much greater than those of the bulk (accelerated by two orders of magnitude from the ratio of the rate constants using the microdroplet and the bulk method). Furthermore, microdroplet phosphonylation can be scaled up to a 1-phenyl-2-dimethylphosphonite-1,2,3,4-tetrahydroisoquinoline amount of 510 mg h-1 by spraying 0.1 mol L-1 N-phenyltetrahydroisoquinoline at 300 μL min-1. These figures of merit make it a promising alternative to classic organic methodologies for the synthesis of organophosphorus compounds.