HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864798Generated: October 31, 2026
Trityl chloride → 6-Bromo-3-trityl-3H-benzooxazol-2-one
https://huagongshe.com/reaction/1864798
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 6-Bromo-2(3H)-benzoxazolone | HCID 29859 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-3-trityl-3H-benzooxazol-2-one | HCID 3097018 | — |
Reaction Steps
To a solution of 6-bromo-3H-benzoxazol-2-one (15 g; ca. 0.07 mol, containing 8-9% 3H-benzooxazol-2-one) and triethylamine (11.1 mL, 0.08 mol) in DCM (250 mL) was added trityl chloride (21.5 g, 0.08 mol). The solution was stirred at room temperature for 18 h and was then washed with distilled water (3×250 mL), brine (250 mL) and dried (MgSO4), filtered and evaporated to give an off-white colored solid. The product was dissolved in refluxing EtOAc then allowed to cool to room temperature with constant stirring for several hours. The solids were collected (21.16 g) and the filtrate was concentrated until precipitation occurred, re-heated (reflux) for several hours and allowed to cool with stirring to encourage a second crystallization (7.88 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625889B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-803e9630e1164f829161b530594885da |
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| Source note | uspto-grants-2009_12 |
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