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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395437Generated: November 2, 2026

2,3-Dihydroxybutanedioic Acid → HCID 54055691, compound

https://huagongshe.com/reaction/2395437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
ReactantBoric AcidHCID 7628—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 54325774HCID 54325774—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54055691HCID 5405569183%

Reaction Steps

To a solution of 0.44 gm (0.91 mMol) 6-(t-butoxycarbonyl)amino-3-(dimethyl)amino-9-triisopropylsilyl-1,2,3,4-tetrahydro-9H-carbazole in 10 mL tetrahydrofuran at 0° C. were added 0.30 gm boric acid followed by 1.5 mL 1M aqueous tetrabutylammonium fluoride. After 3 hours the reaction mixture was added to dilute aqueous tartaric acid and the resulting mixture extracted several times with dichloromethane. The remaining aqueous phase was made basic with dilute aqueous sodium hydroxide and extracted well with dichloromethane. This organic phase was dried over sodium sulfate and concentrated under reduced pressure. This residue was subjected to radial chromatography (2 mm silica gel), eluting with 96:4 chloroform:methanol containing 5% ammonium hydroxide. Fractions shown to contain product were combined and concentrated under reduced pressure to give 0.246 gm (83%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814653
Source datasetuspto-grants-1998_09
ORD IDord-c01c1c48c8834e01b97d31b3dace2f4a
Source noteuspto-grants-1998_09