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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916363Generated: November 3, 2026

2-Chloro-5-nitroanisole → 2-Methoxy-4-nitrobenzenethiol

https://huagongshe.com/reaction/1916363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitroanisoleHCID 70519—
ReactantSodium sulfide nonahydrateHCID 73972—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Methoxy-4-nitrobenzenethiolHCID 22148741—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of 2-chloro-5-nitroanisole (1.00 g; 5.33 mmol) in 10 mL of ethanol at rt was added a solution of sodium sulfide nonahydrate (1.30 g; 5.41 mmol) in 1.4 mL of water and 0.8 mL of ethanol in three portions over 3 minutes. The resulting suspension was heated at 100° C. for 10 min. The suspension was cooled and concentrated under reduced pressure to a dark solid which was used immediately in the next step. HPLC 2.23 min retention time; LCMS (ES): m/z 186 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618115B2
Source datasetuspto-grants-2013_12
ORD IDord-f52fcc9dce9340b5a6400a2f4c841b42
Source noteuspto-grants-2013_12