HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538519Generated: October 30, 2026
Boron tribromide → HCID 59402755, compound
https://huagongshe.com/reaction/538519
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 59402900 | HCID 59402900 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59402755 | HCID 59402755 | 3% |
Reaction Steps
Compound 2,6-difluoro-3-[5-(4-methoxy-phenyl)-benzothiazol-2-ylmethoxy]-benzamide (0.095 g, 0.223 mmol) was dissolved in 5 ml of DCM and cooled to −70° C. To this, BBr3 (0.1 ml 0.156 mmol) was added drop wise. After complete addition, reaction mixture was stirred at r.t. for 30 min. The reaction mixture was quenched with MeOH. Reaction mixture was concentrated and purified by column chromatography to obtain (0.0025 g, 3%) compound as white solid. 1H NMR (DMSO-d6, 400 MHz); δ 5.70 (s, 2H), 6.88 (d, 1H, J=8.4 Hz (o-coupling), 7.10 (m, 1H), 7.41 (m, 2H), 7.60 (d, 2H, J=8.8 Hz, (o-coupling), 7.71 (d, 2H), 7.89 (broad s, 1H), 8.13-8.17 (m, 2H), 9.62 (broad s, 1H); MS ES+ (413.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865736B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c1b9d42e26074faa91502f18d8b3fafb |
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| Source note | uspto-grants-2014_10 |
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