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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808676Generated: October 26, 2026

Tetrahydrofuran → 1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene

https://huagongshe.com/reaction/1808676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,3,5-Tris(4-hydroxyphenyl)benzeneHCID 348148—
ReactantBromo-t-butylacetateHCID 21584499—
ReactantPotassium tert-butoxideHCID 23665647—
Product1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzeneHCID 68862158—

Reaction Steps

18 g of 1,3,5-tris(4-hydroxyphenyl)benzene was dissolved in 500 ml of tetrahydrofuran. 6 g of potassium t-butoxide was added and the mixture was stirred at room temperature for five minutes. After the addition of 10 g of bromo-t-butylacetate dropwise, the mixture was stirred for six hours while heating at 60° C. After evaporating tetrahydrofuran under reduced-pressure, the reaction product was extracted with 300 ml of dichloromethane, purified using a silica gel column, and dried to obtain 4.6 g of 1-(t-butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361691B2
Source datasetuspto-grants-2013_01
ORD IDord-465366b4c54a446ba9b337ebada64dcf
Source noteuspto-grants-2013_01