HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560277Generated: October 29, 2026
Hydrochloric Acid → Methyl 3,4-dihydro-2H-1,4-benzoxazine-5-carboxylate
https://huagongshe.com/reaction/560277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59153381 | HCID 59153381 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3,4-dihydro-2H-1,4-benzoxazine-5-carboxylate | HCID 14373654 | — |
Reaction Steps
Boron trifluoride diethyl etherate (7.10 mmol) is added dropwise to a mixture of 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-5-carboxylic acid methyl ester (3.38 mmol) in THF (10 mL) to keep the temperature below 5° C. After 20 min sodium borohydride (7.10 mmol) is added and the mixture is stirred at 5° C. for 90 min. EtOAc (6.0 mL) and aq. HCl (1.0 M, 6.0 mL) are added dropwise. The mixture is made basic by addition of aq. Na2CO3 solution, the layers are separated and the aq. layer is extracted with EtOAc. The combined organic layers are dried over MgSO4 and concentrated in vacuo to give a crude product which is purified by FC (heptane to heptane/EtOAc 3/7). LC-MS: tR=0.90 min; [M+CH3CN+H]+=235.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063099B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-dc3db26fba2c40cf8858d201287ed491 |
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| Source note | uspto-grants-2011_11 |
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