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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879277Generated: October 31, 2026

Toluene → HCID 71503471, compound

https://huagongshe.com/reaction/1879277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantL-Pyroglutamic AcidHCID 7405—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 71503470HCID 71503470—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 71503471HCID 71503471—

Reaction Conditions

Temperature-70 °C

Reaction Steps

Nucleoside 102-U (3.01 g, 5.50 mmol) was coevaporated with an. toluene (15 mL). The resulting residue was dissolved in an. DCM (150 mL) along with an. Pyr. (4.4 mL) and the mixture was cooled to −70° C. Benzoyl chloride (700 μL, 6 mmol) was slowly added to the reaction mixture and stirred for 1 h at −70° C. EtOH (5 mL) was added to the solution and subsequently allowed to reach rt. The reaction mixture was washed with sat. aq. NaHCO3 (3×100 mL) and brine (100 mL). The combined aqueous phase was back extracted with CH2Cl2 (100 mL). The organic phases were combined and evaporated. The resulting residue was purified by column chromatography (3.5% MeOH in DCM) affording the product 103-U as a white foam after evaporation of the solvents.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314227B2
Source datasetuspto-grants-2012_11
ORD IDord-702ff37abb454981a31741ab5f755720
Source noteuspto-grants-2012_11