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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338455Generated: October 30, 2026

Boron Trichloride → HCID 86698789, compound

https://huagongshe.com/reaction/338455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 86698788HCID 86698788—
SolventDichloromethaneHCID 6344—
ProductHCID 86698789HCID 8669878925%

Reaction Steps

To a 0° C. slurry of methyl 5-[4-(3-Benzyloxymethyl-oxetan-3-yl)-phenyl]-6-chloro-1H-indole-3-carboxylate (200 mg, 0.433 mmol) in DCM (5 mL) was added boron trichloride (1.73 mL, 1.0M in DCM, 1.73 mmol) via syringe, and the mixture was allowed to warm to room temperature over five hours. The reaction mixture was concentrated to dryness, diluted with ethyl acetate (200 mL), washed with water (10 mL) and saturated brine (10 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to afford an orange film, which was purified by flash chromatography (12 g silica, 20-100% ethyl acetate/heptane, 38 column volumes). Product fractions were combined and concentrated in vacuo to afford the title compound as a colorless oil (40 mg, 25% yield). MS (ES+) 372 (M+H)+; 1H NMR (500 MHz, CD3OD) δ ppm 8.00-8.04 (m, 2H), 7.60 (s, 1H), 7.44-7.55 (m, 4H), 4.10 (s, 2H), 3.95-4.07 (m, 4H), 3.88 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-7a3db92264d84f48b5a1ffccdc8cbfd9
Source noteuspto-grants-2014_11