HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419161Generated: October 29, 2026
Dimethyl Sulfide → (3,4-Dihydro-2H-1,4-benzoxazin-8-yl)methanol
https://huagongshe.com/reaction/419161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acid | HCID 18354941 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3,4-Dihydro-2H-1,4-benzoxazin-8-yl)methanol | HCID 53414296 | — |
Reaction Steps
To a suspension of 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (1.51 g, 7.8 mmol) in anhydrous THF (10 mL) was added BH3.Me2S (2 M in THF, 10 mL, 20 mmol) dropwise under nitrogen at 0° C. The resulted mixture was allowed to rise to r.t., and the reaction was continued to be carried out at this temperature overnight. Then, saturated aqueous NH4Cl (30 mL) was added in, and the resulted mixture was extracted with EtOAc (200 mL×2). The combined organic layers were washed with saturated aqueous NaHCO3 solution (30 mL), brine (30 mL), dried (Na2SO4) and filtered before it was concentrated under reduced pressure. The resulted crude product (3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-methanol, which was utilized in the following step without further purification. MS m/z: 166.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093247B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-580994ff0b85433b803a6efdff0bbdab |
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| Source note | uspto-grants-2012_01 |
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