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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376911Generated: October 31, 2026

1,2-Dichloroethane → HCID 15896052, compound

https://huagongshe.com/reaction/376911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylformamideHCID 6228—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 15896051HCID 15896051—
ProductHCID 15896052HCID 1589605237%

Reaction Steps

[Octyl-(toluene-4-sulfonyl)amino]-acetic acid (4.0 g, 0.012 mol) was taken up in DMF (150 ml) and treated at room temperature with NMM (1.55 ml, 0.014 mol) followed by EDC (2.92 g, 0.015 mol). The reaction mixture was allowed to stir for 15 minutes at room temperature before the addition of HOBt (2.1 g, 0.016 mol). The reaction mixture was left to stir for a further 20 minutes before a mixture of O-benzyihydroxylamine hydrochloride (1.87 g, 0.012 mol) and NMM (2.6 ml, 0.024 mol) in DMF (50 ml) was added. The reaction mixture was allowed to stir at room temperature for a further 48 h. The DMF was removed under reduced pressure and the resulting crude oil was dissolved in ethyl acetate (200 ml). The solution was washed consecutively with 1M HCl, 0.5M Na2CO3 and brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The resulting crude oil was purified by flash chromatography (silica gel, 10% methanol in dichioromethane) to give an oil which was further purified by flash chromatography (silica gel, 20% ethyl acetate in hexane) to give the title compound as a white solid (1.91 g, 37%). 1H NMR: δ (CDCl3), 9.39 (1H, br s), 7.65 (2H, d, J=8.2 Hz), 7.45-7.20 (7H, m), 4.91 (2H, s), 3.67 (2H, br s), 3.07 (2H, dd, J=7.5, 7.9 Hz), 2.40 (3H, s), 1.50-1.33 (2H, m), 1.31-1.10 (10H, m) and 0.86 (3H, t, J=6.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022898
Source datasetuspto-grants-2000_02
ORD IDord-0bcdc944fc034799b93760ddad77979e
Source noteuspto-grants-2000_02