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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176683Generated: November 1, 2026

Sodium Hydroxide → 3,4-dihydro-2H-1,4-benzothiazine-6-carbaldehyde

https://huagongshe.com/reaction/1176683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylateHCID 699501—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3,4-dihydro-2H-1,4-benzothiazin-6-ylmethanolHCID 59560616—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3,4-dihydro-2H-1,4-benzothiazine-6-carbaldehydeHCID 2187369358%

Reaction Steps

(3,4-Dihydro-2H-benzo[1,4]thiazin-6-yl)-methanol. To a solution of 3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid methyl ester (750 mg, 3.4 mmol) in Et2O (32 mL) was added LiAlH4 (240 mg, 6.3 mmol) and the resulting suspension was stirred at RT for 24 h. The reaction mixture was cooled to 0° C. and treated with H2O (0.5 mL), 15% aq. NaOH (0.5 mL), and H2O (1.5 mL). The resulting suspension was filtered. The filtrate was concentrated to provide 340 mg (58%) of the title compound as an amber oil. MS (ESI): exact mass calculated for C9H11NOS, 181.06; m/z found, 182.1 [M+H]+. 1H NMR (500 MHz, CDCl3): 6.96 (d, J=7.9, 1H), 6.60 (dd, J=7.9, 1.6, 1H), 6.49 (d, J=7.9, 1H), 4.52 (s, 2H), 3.65-3.62 (m, 2H), 3.06-3.04 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842810B2
Source datasetuspto-grants-2010_11
ORD IDord-ffbfe18edd0c4418a72f9e5af3daaeea
Source noteuspto-grants-2010_11