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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424681Generated: November 3, 2026

1-(Azidomethyl)-3-(trifluoromethyl)benzene → HCID 44517958, compound

https://huagongshe.com/reaction/1424681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Azidomethyl)-3-(trifluoromethyl)benzeneHCID 21282668—
ReactantHCID 44517957HCID 44517957—
ProductHCID 44517958HCID 44517958—

Reaction Steps

Synthesized from 4-(3-iodoprop-2-ynyloxy)-3-methoxybenzaldehyde and 3-trifluoromethyl-benzylazide using general procedure; 0.398 g, 0.769 mmol, 97%; mp=130-134° C. (dec.); IR (υ[cm−1]) 3123, 1702, 1689, 1588, 1506, 1329, 1262, 1133, 1123, 994, 792; 1H NMR (600 MHz, CDCl3) δ=9.83 (s, 1H), 7.59 (d, J=7.6, 1H), 7.56 (s, 1H), 7.47 (t, J=7.7, 1H), 7.41 (dd, J=15.8, 6.7, 2H), 7.39 (s, 1H), 7.21 (d, J=8.1, 1H), 5.62 (s, 2H), 5.27 (s, 2H), 3.88 (s, 3H); 13C NMR (151 MHz, CDCl3) δ=191.2, 153.1, 150.5, 147.5, 135.0, 131.6, 131.6 (q, J=32.7), 131.1, 129.9, 126.7, 125.9 (q, J=3.6), 125.1 (q, J=3.7), 123.9 (q, J=272.4), 113.5, 109.7, 81.2, 62.9, 56.3, 54.0; HRMS (ESI-TOF) (m/z): [M+H]+ calcd for C19H16F3IN3O3, 518.0183; found 518.0186.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927736B2
Source datasetuspto-grants-2015_01
ORD IDord-c5b722cd0aee41e68ea4b315790b4fe7
Source noteuspto-grants-2015_01