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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811571Generated: October 30, 2026

2-Mercaptoethanol → 2-(6-Methyl-5-nitro-pyridin-2-ylsulfanyl)-ethanol

https://huagongshe.com/reaction/1811571

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Chloro-2-methyl-3-nitropyridineHCID 253123—
Product2-(6-Methyl-5-nitro-pyridin-2-ylsulfanyl)-ethanolHCID 11424429—

Reaction Steps

To an ice-cooled solution of 6-chloro-2-methyl-3-nitropyridine (2.17 g, 13 mmol) in 2-mercaptoethanol (5 mL, 71 mmol), potassium hydroxide (1.52 g, 27 mmol) was added. Mixture was stirred at room temperature for 2 h and then extracted with NaOH solution and CH2Cl2. Organic phases were dried over MgSO4, filtered, and concentrated to give 2-(6-methyl-5-nitro-pyridin-2-ylsulfanyl)-ethanol as a brown oil (60% pure, 3.25 g, 72%). 1HNMR (CDCl3, 400 MHz) δ 2.87-2.90 (m, 6H), 3.43-3.46 (t, J=5.6 Hz, 2H), 7.22-7.24 (d, J=8.7 Hz, 1H), 8.15-8.17 (d, J=8.7 Hz, 1H). Exact mass calculated for C8H10N2O3S 214.04 found 215.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362248B2
Source datasetuspto-grants-2013_01
ORD IDord-5b14a028bcb14667a47111836e646bd6
Source noteuspto-grants-2013_01