HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912608Generated: October 30, 2026
HCID 59281523, compound → 6-Bromo-3,4-dihydro-5-methyl-2H-1,4-benzoxazine
https://huagongshe.com/reaction/1912608
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59281523 | HCID 59281523 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Bromo-3,4-dihydro-5-methyl-2H-1,4-benzoxazine | HCID 59578662 | — |
Reaction Steps
An ice cold mixture of 6-bromo-5-methyl-2H-1,4-benzoxazin-3(4H)-one (3.05 g, 12.59 mmol) in tetrahydrofuran (THF) (40 mL) was treated with borane tetrahydrofuran complex (1.0 M solution in tetrahydrofuran (18.88 mL, 18.88 mmol) and the mixture was stirred at ambient temperature for 150 minutes. The mixture was cooled to 0° C. and then quenched slowly with 1N NaOH (30 mL). The mixture was extracted with ethyl acetate, then washed with 1N NaOH, dried over sodium sulfate, filtered and then concentrated to a thick dark brown oil. The material was purified on silica gel (95:4:1 dichloromethane/methanol/ammonium hydroxide, gradient) to afford an off-white solid: 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 6.87 (d, J=8.6 Hz, 1 H), 6.57 (d, J=8.8 Hz, 1 H), 4.31-4.15 (m, 2 H), 3.56-3.38 (m, 2 H), 2.22 (s, 3 H); LC/MS (m/z) ES+=228 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609653B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-b8f1e14531f940b28ab81ba3399cdad7 |
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| Source note | uspto-grants-2013_12 |
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