Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 4-(2-methoxyphenyl)morpholine | HCID 10655409 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-morpholinophenol | HCID 2795394 | 80% |
Reaction Steps
To a solution of 4-(2-methoxyphenyl)morpholine (200 mg, 1.02 mmol) in CH2Cl2 (20 mL) was added BBr3 (1 mL) at 0° C. The mixture was stirred for 2 h at 0° C. The mixture was then added drop wise to ice-water (50 mL) and the mixture treated with CH2Cl2 (2×20 mL). The combined organic layers were washed with brine (30 mL), dried over Na2SO4 and concentrated to give the yellow solid which was used in next step without further purification (165 mg Yield 80%). LCMS (m/z): 180.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266836B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-abbf6dcb699f4c548a3b791722325087 |
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| Source note | uspto-grants-2016_02 |
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