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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885671Generated: October 25, 2026

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

https://huagongshe.com/reaction/885671

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 numberUS08242275B2
Source datasetuspto-grants-2012_08
ORD IDord-e6fb8601138e46218f2c79bb4451c891
Source noteuspto-grants-2012_08