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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609721Generated: October 29, 2026

HCID 10049710, compound → HCID 9979889, compound

https://huagongshe.com/reaction/1609721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10049710HCID 10049710—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
ProductHCID 9979889HCID 9979889—

Reaction Steps

3,5-Dichloro-4-(3'-isopropyl-4'-t-butyldimethylsiloxyphenoxy)-nitrobenzene and 1.15 g of 10% platinum on carbon in 200 ml of ethanol is hydrogenated on a Parr shaker. Catalyst is removed by tinting through Celite and the filtrate stripped to afford 3,5-dichloro4-(3'-isopropyl-4'-t-butyldimethylsiloxyphenoxy)-aniline. This is dissolved with 3.08 ml of ethyl bromoacetate and 3.43 g of diisopropylethylamine in 50 ml dimethylformamide and heated at 140° for 18 hours. Solvent is removed with high vacuum and the residue taken up in ethyl acetate and extracted twice with water. The ethyl acetate is dried, filtered and stripped to give crude product. Chromatography on silica gel with 85:15 to 80:20 hexane:ethyl acetate as eluent affords ethyl N-[3,5-dichloro-4-(3'-isopropyl-4'-t-butyldimethylsiloxyphenoxy)phenyl]aminoacetate. NMR (CDCl3): δ0.2 (6H,s), 1.0 (9H,s), 1.2 (6H,d), 1.3 (3H,t), 3.3 (1H,m), 3.9 (2H,d), 4.3 (2H,q), 4.4 (1H,t), 6.4 (1H,d of d), 6.6 (2H,s), 6.6 (1H,d), 6.9 (1H,d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401772
Source datasetuspto-grants-1995_03
ORD IDord-dfbfce66b86d4870aa9610f5caf8ac18
Source noteuspto-grants-1995_03