Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium CarbonateHCID 10340—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59153381HCID 59153381—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3,4-dihydro-2H-1,4-benzoxazine-5-carboxylateHCID 14373654—

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063099B2
Source datasetuspto-grants-2011_11
ORD IDord-dc3db26fba2c40cf8858d201287ed491
Source noteuspto-grants-2011_11