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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507031Generated: October 31, 2026

HCID 86729448, compound → ethyl 2-((4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-5-yl)oxy)acetate

https://huagongshe.com/reaction/1507031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86729448HCID 86729448—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Productethyl 2-((4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-5-yl)oxy)acetateHCID 8672944776%

Reaction Conditions

Temperature27 °C

Reaction Steps

A solution of ethyl 2-((4-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-5-yl)oxy)acetate (100 mg, 0.377 mmol) in anhydrous THF (3 mL) was cooled to 0° C. and BH3-Me2S (0.1 mL) added. The solution was stirred at 27° C. for 6 h, diluted with methanol and concentrated. The residue was partitioned between ethyl acetate (30 mL) and water (20 mL), the organic layer washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product was purified by preparative TLC. (72 mg, yield 76%) MS (ESI+) e/z: 252.2 [M+1]+. 1H NMR (CDCl3, 400 MHz), δ ppm: 6.87-6.76 (m, 1H), 6.62-6.52 (m, 1H), 6.40-6.28 (m, 1H), 4.70 (s, 2H), 4.34-4.22 (m, 2H), 4.18-4.06 (m, 2H), 3.21-3.07 (m, 2H), 2.99-2.85 (m, 3H), 1.33-1.25 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221794B2
Source datasetuspto-grants-2015_12
ORD IDord-5de07be429844c5f9359638a41b93fc0
Source noteuspto-grants-2015_12