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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279977Generated: November 1, 2026

Tetrahydrofuran → HCID 86707588, compound

https://huagongshe.com/reaction/2279977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 86707589HCID 86707589—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
ProductHCID 86707588HCID 86707588—

Reaction Conditions

Temperature70 °C

Reaction Steps

5.40 g (7.82 mmol) 3-benzyloxy-propionic acid-4″-(3-benzyloxy-propionyloxy)-5′-(2-methoxy-ethoxymethoxy)-[1,1′;3′,1″]terphenyl-4-yl ester are dissolved in 40 ml isopropanol and 10 ml THF and after addition of 1.97 g (7.82 mmol) pyridiniumtosylate are stirred for 60 h at 70° C. After cooling to RT the mixture is diluted with MTB ether, washed with sat. aq. sodium chloride solution and dried over sodium sulfate. The solvent is removed in vacuo and the residue is hydrogenated in 40 ml THF on Pd/activated charcoal until the reaction is completed. The solvent is removed in vacuo and the crude product is recrystallized from dichloromethane, to give 3-hydroxy-propionic acid-5′-hydroxy-4″-(3-hydroxy-propionyloxy)-[1,1′;3′,1″]terphenyl-4-yl ester as colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133395B2
Source datasetuspto-grants-2015_09
ORD IDord-987733ee9f37406fba736152d460dbee
Source noteuspto-grants-2015_09