Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-Bromo-1,4-benzenediol | HCID 68502 | — |
Reaction Steps
To a solution of hydroquinone Q-1 (10 g, 90.90 mmol) in MTBE (methyl tert-butyl ether) (100 mL) at −5° C. was added bromine (17.4 g, 90.90 mmol). The reaction mixture was stirred at 0° C. for 30 min. Solvent was removed in vacuo and the crude product was purified by column chromatography (SiO2, 2% MeOH—CHCl3) to afford compound Q-2 (13 g, 75%) as a solid. TLC Rf=0.6 (CHCl3-MeOH, 9:1); 1H NMR (CDCl3) δ 6.94 (app d, 1H), 6.88 (d, J=8.7 Hz, 1H), 6.72 (dd, J=8.7, 2.8 Hz, 1H), 5.19 (s, 2H) (Synlett 2000, 11, 1561-1564).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614237B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-0ccd451e670042eaa2c5e5a153cc8d9f |
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| Source note | uspto-grants-2013_12 |
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