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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866005Generated: October 29, 2026

HCID 10049710, compound → HCID 9979889, compound

https://huagongshe.com/reaction/866005

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 filtration through Celite and the filtrate stripped to afford 3,5-dichloro-4-(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 numberUS05569674
Source datasetuspto-grants-1996_10
ORD IDord-0a4ace2a719c4a57922b766b92f3adcc
Source noteuspto-grants-1996_10