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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054540Generated: November 1, 2026

Dichloromethane → HCID 86705754, compound

https://huagongshe.com/reaction/1054540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 67818597HCID 67818597—
ProductHCID 86705754HCID 86705754—

Reaction Steps

4-[6-chloro-5-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,3-benzodiazol-2-yl]butan-1-ol (1.00 g, 2.36 mmol) was dissolved in DCM (30 ml) and Dess-Martin reagent (1.10 g, 2.60 mmol) was added at r.t. The reaction was left for 4 hrs. The reaction was quenched by the addition of 1M Na2S2O3 solution (10 ml), sat. NaHCO3 solution (40 ml) and DCM (80 ml). The organic layer was separated and the aqueous layer was extracted with DCM (3×80 ml). The combined organic layers were dried over MgSO4, filtered and concentrated in vacuo to give the crude product. The product was purified by silica flash column chromatography eluting with EtOAc:heptanes (1:1) as a light orange oil (0.53 g, 38%): MS (ESI+) for C18H24ClF3N2O2Si m/z 422.05 [M+H]+; LC purity 72% (ret. time, 1.81 min); 1H NMR (250 MHz, CHLOROFORM-d) δ ppm −0.21-0.21 (9H, m), 0.77-1.01 (2H, m), 2.17-2.36 (2H, m), 2.64-2.86 (2H, m), 3.02 (2H, td, J=7.39, 3.20 Hz), 3.35-3.74 (2H, m), 5.39-5.60 (2H, m), 7.34-8.18 (2H, m), 9.82 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394310B2
Source datasetuspto-grants-2016_07
ORD IDord-841bb0245a70470a98a20d85938773f5
Source noteuspto-grants-2016_07