Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431725Generated: November 1, 2026

Carbon Tetrachloride → Methyl 3-[2-benzyloxy-5-(2-chloroethyl)-4-nitroanilino]-4,4,4-trifluoro-2-butenoate

https://huagongshe.com/reaction/431725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 3-[2-benzyloxy-5-(2-hydroxyethyl)-4-nitroanilino]4,4,4-trifluoro-2-butenoateHCID 69547699—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-[2-benzyloxy-5-(2-chloroethyl)-4-nitroanilino]-4,4,4-trifluoro-2-butenoateHCID 69546885—

Reaction Steps

Triphenylphosphine (2.57 g, 9.77 mmol), CCl4 (2.83 mL, 29.3 mmol), and dry CH2Cl2 (55 mL) were added to methyl 3-[2-benzyloxy-5-(2-hydroxyethyl)-4-nitroanilino]4,4,4-trifluoro-2-butenoate (2.10 g, 4.89 mmol) in a round bottom flask. The yellow solution was flushed with N2 and stirred overnight. The solution was checked by TLC (20% ethyl acetate/petroleum ether) and then concentrated under reduced pressure. The residue was purified on a silica gel column run in 10% ethyl acetate/petroleum ether solvent system to give methyl 3-[2-benzyloxy-5-(2-chloroethyl)-4-nitroanilino]-4,4,4-trifluoro-2-butenoate. Total yield: 1.25 g (2.71 mmol, 57%). M.p.=105-110° C. TLC (20% ethyl acetate /petroleum ether) Rf320.69.500 MHz 1H-NMR (CDCl3) 10.04 (s, 1H), 7.72 (s, 1H), 7.48 (d, 7.5, 2H), 7.41 (t, 7.5, 2H), 7.35 (t, 7.5, 1H), 7.14 (s, 1H), 5.63 (s, 1H), 5.23 (s, 2H), 3.80 (t, 6.5, 2H), 3.75 (s, 3H), 3.33 (t, 6.5, 2H). IR (neat) 2415, 3050, 2956, 1730, 1687, 1640, 1615, 1585, 1530, 1334, 1296, 1215, 1143, 1024, 815, 739, 696. EI-MS (relative intensity) 458 (M+, 6). Accurate mass for C20H18O5N235ClF3: calcd. 458.0856, obsd. 458.0853.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660742B2
Source datasetuspto-grants-2003_12
ORD IDord-b3123db0852d438b995a63447463b3d3
Source noteuspto-grants-2003_12