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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648448Generated: October 25, 2026

Benzene → HCID 21832179, compound

https://huagongshe.com/reaction/1648448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant2-Amino-1-(naphthalen-2-yl)ethan-1-olHCID 2735379—
ReactantSodium borohydrideHCID 4311764—
Reactant5-[4-(2-Oxopropoxy)benzyl]thiazolidine-2,4-dioneHCID 21832150—
SolventMethanolHCID 887—
ProductHCID 21832179HCID 21832179—

Reaction Steps

A procedure similar to that described in Preparation 10, below, was followed, but using 520 mg of 2-amino-1-(2-naphthyl)ethanol [prepared as described in Preparation 8], 650 mg of 5-[4-(2-oxopropoxy)benzyl]thiazolidine-2,4-dione [prepared as described in Preparation 9], 150 ml of benzene, 100 ml of absolute methanol and 1.25 g of sodium borohydride, to give the title compound in crude form. This crude product was then purified by column chromatography through silica gel, using a 5:1 by volume mixture of ethyl acetate and ethanol as the eluent, to give 490 mg of the title compound melting at between 115° C. and 145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436257
Source datasetuspto-grants-1995_07
ORD IDord-71c05cdd02a34ea3a5c210a4b422dc44
Source noteuspto-grants-1995_07