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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898170Generated: October 31, 2026

Dimethyl Sulfide → (3,4-Dihydro-2H-1,4-benzoxazin-8-yl)methanol

https://huagongshe.com/reaction/1898170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acidHCID 18354941—
SolventTetrahydrofuranHCID 8028—
Product(3,4-Dihydro-2H-1,4-benzoxazin-8-yl)methanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519135B2
Source datasetuspto-grants-2013_08
ORD IDord-18d8d599baf34037b230543b9a226415
Source noteuspto-grants-2013_08