HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228982Generated: October 30, 2026
HCID 22261246, compound → HCID 22261247, compound
https://huagongshe.com/reaction/2228982
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22261246 | HCID 22261246 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22261247 | HCID 22261247 | 73.3% |
Reaction Steps
A solution of 2-(3-bromophenyl)-5-methyl-4-oxazoleacetic acid (39.1 g, 0.13 mol) in dry THF (175 mL) was treated dropwise with borane-THF complex (227 mL of a 1.0 M solution in THF, 1.3 mol) over 2 h (reaction temperature to 35° C.). After stirring 2 h at room temperature under N2, the reaction was quenched with slow addition of methanol (60 mL) and stirred overnight at room temperature. The reaction was diluted with 1 N NaOH (50 mL) and extracted with CH2Cl2 (2×200 mL). The organic layer was washed with H2O (3×100 mL), dried (MgSO4), and the solvent removed in vacuo to give 38.7 g of crude product that was recrystallized from toluene (200 mL, wash solid with cold hexanes) to give 26.9 g (72%) of 2-(3-bromophenyl)-5-methyl-4-oxazoleethanol as a white powder. Mp 92-93° C.; 1H NMR (300 MHz, d6-DMSO) δ7.99 (s, 1H), 7.88 (d, J=7.7 Hz, 1H), 7.64 (d, J=7.7 Hz, 1H), 7.44 (t, J=7.7 Hz, 1H), 4.61 (t, J=5.5 Hz, OH), 3.63 (q, J=5.5 Hz, 2H), 2.60 (t, J=6.6 Hz, 2H), 2.32 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06417212B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-aae8868c1d2a47a69d162b408348228d |
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| Source note | uspto-grants-2002_07 |
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