HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338455Generated: October 30, 2026
Boron Trichloride → HCID 86698789, compound
https://huagongshe.com/reaction/338455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 86698788 | HCID 86698788 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86698789 | HCID 86698789 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889730B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-7a3db92264d84f48b5a1ffccdc8cbfd9 |
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| Source note | uspto-grants-2014_11 |
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