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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293000Generated: November 3, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 58635311, compound

https://huagongshe.com/reaction/1293000

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantHCID 86594471HCID 86594471—
SolventWater methylene chlorideHCID 21908982—
ProductHCID 58635311HCID 58635311—
ProductHCID 86594470HCID 86594470—

Reaction Steps

To a solution of {[(2R)-2-azido-4-(4-methoxyphenoxy)butyl]oxy}(tert-butyl)dimethylsilane (4.7 g, 12.86 mmol) in 19:1 DCM/water at 0° C. was added DDQ (2,3-Dichloro-5,6-dicyano-1,4-benzoquinone) (3.5 g, 15.43 mmol, 1.2 eq) and the mixture was stirred (from 0° C. to rt) until all starting material disappeared as indicated by TLC (thin layer chromatography) analysis. Most DCM was then removed in vacuo and the residue was dissolved in ethyl acetate. The ethyl acetate solution was washed with water and saturated NaHCO3 repeatedly until a pale yellow organic solution was obtained. The organic solution was dried and the crude was purified by silica gel chromatography 5% acetone/toluene) to give the desired product (3R)-3-azido-4-{[tert-butyl(dimethyl)silyl]oxy}butan-1-ol. 1H NMR (400 MHz, Acetone-d6): δ 3.89 (1H, dd), 3.73-3.65 (5 H, m), 1.76-1.68 (1 H, m), 1.62-1.54 (1 H, m), 0.94 (9 H, s), 0.13 (6 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238710B2
Source datasetuspto-grants-2007_07
ORD IDord-c18f7956573f4f5db4aa65b2b69df7da
Source noteuspto-grants-2007_07