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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474247Generated: October 29, 2026

Trifluoroacetic acid → HCID 66665326, compound

https://huagongshe.com/reaction/474247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86668105HCID 86668105—
SolventDichloromethaneHCID 6344—
ProductHCID 66665326HCID 6666532689%

Reaction Steps

To an ice-cold solution of tert-butyl (2-(2-cyano-5-nitrophenoxy)ethyl)carbamate (4 g, 13.02 mmol) in DCM (20 mL) was added TFA (10 mL). The reaction mixture was stirred at rt for 60 min. The solvent was removed under reduced pressure and treated with saturated sodium bicarbonate solution (10 mL) and extracted with ethyl acetate (2×25 mL). The organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure to get 2-(2-aminoethoxy)-4-nitrobenzonitrile (2.4 g, 89%) as a yellow solid. LC-MS (M+H)+=208.0. 1H NMR (400 MHz, CDCl3) δ ppm 7.89 (1H, d, J=8.4 Hz), 7.83 (1H, s), 7.76 (1H, d, J=8.4 Hz), 4.23 (2H, t, J=5.2 Hz), 3.22 (2H, t, J=5.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637523B2
Source datasetuspto-grants-2014_01
ORD IDord-1121d58c97a0446086c81cc8a9156a91
Source noteuspto-grants-2014_01