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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851922Generated: October 30, 2026

1,3-Cyclohexadiene → HCID 44283041, compound

https://huagongshe.com/reaction/851922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-CyclohexadieneHCID 11605—
ReactantHCID 86600475HCID 86600475—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 44283041HCID 44283041—

Reaction Steps

To a solution of N-benzyloxy-N-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-ylmethyl)-formamide (0.17 mmol) in EtOH (12 mL) is added Pd/C (10%) (88.5 mg) followed by cyclohexadiene (1.8 mL). The reaction mixture is stirred at room temperature for 12 hours and the final product N-hydroxy-N-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-ylmethyl)-formamide is obtained by preparative LC/MS using 1 to 99% ACN as gradient. 1H NMR (400 MHz, MeOD): δ 8.48 (s, 0.4H), 7.97 (s, 0.6H), 7.49 (m, 2H), 7.19 (m, 2H), 4.03 (m, 2H), 3.5 (dd, 1H). MS: (ES+): 239.1[M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253164B2
Source datasetuspto-grants-2007_08
ORD IDord-7a22038ad1fa43b4a0351b1b519d8390
Source noteuspto-grants-2007_08