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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765052Generated: October 27, 2026

Trifluoroacetic acid → 3,4-Dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/1765052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 2,3-dihydro-1,4-benzoxazine-4-carboxylateHCID 15348605—
SolventDichloromethaneHCID 6344—
Product3,4-Dihydro-2H-1,4-benzoxazineHCID 585096—

Reaction Steps

To a solution of dichloromethane (10 mL) containing N-(tertbutoxycarbonyl)-2,3-dihydro-benzo[1,4]oxazine (0.438, 1.86 mmol) at 0° C. was added slowly trifluoroacetic acid (1.0 mL, 7.44 mmol). The reaction mixture was stirred at this temperature during 5 h, then the solvent was removed in vaccuo. The crude product was dissolved in EtOAc (15 mL) and washed successively with 10% Na2CO3 solution and water. The organic layer was dried over MgSO4 and the solvent was removed under reduce pressure. The title compound was obtained pure as brown oil (0.245 g, 98%). Rf=0.31 (petrol/ether 5/5); LCMS m/z 136 ([M+1]+); 1H NMR (300 MHz, CDCl3): δ 3.43 (4H, m); 3.54 (1H, s); 4.27 (4H, m); 6.60-6.82 (4H, m); 13C NMR (75 MHz, CDCl3): δ 43.4; 67.7; 118.1; 119.2; 121.3; 123.7; 136.1; 146.6. IR (film): 3375; 1498; 741 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226918B2
Source datasetuspto-grants-2007_06
ORD IDord-a91af5e6f4b642fba07db9ed9902e3f8
Source noteuspto-grants-2007_06