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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972025Generated: October 30, 2026

2,2-Bis{4-[2-hydroxy-3-(7,7,9,9-tetramethyl-2,4-dioxo-1,3,8-triazaspiro[4.5]dec-3-yl)propoxy]phenyl}propane → 2,2-Bis{4-[2-acetoxy-3-(8-acetyl-7,7,9,9-tetramethyl-2,4-dioxo-1,3,8-triazaspiro[4.5]dec-3-yl)propoxy]phenyl}propane

https://huagongshe.com/reaction/972025

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Bis{4-[2-hydroxy-3-(7,7,9,9-tetramethyl-2,4-dioxo-1,3,8-triazaspiro[4.5]dec-3-yl)propoxy]phenyl}propaneHCID 23462718—
SolventAcetic AnhydrideHCID 7918—
Product2,2-Bis{4-[2-acetoxy-3-(8-acetyl-7,7,9,9-tetramethyl-2,4-dioxo-1,3,8-triazaspiro[4.5]dec-3-yl)propoxy]phenyl}propaneHCID 20396799—

Reaction Steps

5 g of 2,2-bis{4-[2-hydroxy-3-(7,7,9,9-tetramethyl-2,4-dioxo-1,3,8-triazaspiro[4.5]dec-3-yl)propoxy]phenyl}propane were heated at 100°-110° C. in 100 ml of acetic anhydride, with stirring, for 6 hours. After completion of the reaction, the reaction mixture was condensed by evaporation under reduced pressure and then 150 ml of benzene were added to dissolve the residue. The benzene solution was washed successively with a 2% w/w sodium carbonate solution and water. The solvent was then removed and the residue was purified by column chromatography through silica gel eluted with a 8:1:1:1 by volume mixture of ethyl acetate, benzene, ethanol, and triethylamine. The desired Compound No. 68 was obtained in the form of white crystals, melting point 147°-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04162246
Source datasetuspto-grants-1979_07
ORD IDord-f0547bc6cba74bea973bcce9b774d0c9
Source noteuspto-grants-1979_07