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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38924Generated: October 26, 2026

1,1,1-Trifluoro-3-iodopropane → N-{[(2S)-7-(Methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methyl}-N-(3,3,3-trifluoropropyl)amine

https://huagongshe.com/reaction/38924

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluoro-3-iodopropaneHCID 156165—
Reactant[(2S)-7-(methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-yl]methylamineHCID 66878351—
SolventAcetonitrileHCID 6342—
ProductN-{[(2S)-7-(Methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methyl}-N-(3,3,3-trifluoropropyl)amineHCID 44470013—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of [(2S)-7-(methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-yl]methylamine (0.31 g, 1.27 mmol), 1,1,1-trifluoro-3-iodopropane (0.16 ml, 1.4 mmol) K2CO3 (0.35 g, 2.5 mmol) and ACN (4 ml) was heated under microwave radiation at 120° C. for 40 min. The product was evaporated to dryness and was purified by preparative HPLC (MeOH/NH3 buffer). Yield: 0.19 g, 44%. The amine was converted to the hydrochloric acid salt and was crystallized from MeOH/Et2O. M.p. 204° C. MS m/z (rel. intensity, 70 eV) 339 (M+, 3), 127 (5), 126 (bp), 79 (4), 51 (4). [α]=−52° (MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524766B2
Source datasetuspto-grants-2013_09
ORD IDord-b5a4e5da5b324af78e2d58cb3e81d15b
Source noteuspto-grants-2013_09