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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461639Generated: October 29, 2026

1-Fluoro-2-nitrobenzene → 5-(2-Nitrophenyl)thiopyrano[3,2-b]indol-4(5H)-one

https://huagongshe.com/reaction/461639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantThiopyrano[3,2-b]indol-4(5H)-oneHCID 20326608—
Product5-(2-Nitrophenyl)thiopyrano[3,2-b]indol-4(5H)-oneHCID 20326622—

Reaction Conditions

Temperature95 °C

Reaction Steps

By the same method as described in Example 7, 8.9 g of thiopyrano [3,2-b]indol-4(5H)-one is alkylated with o-fluoronitrobenzene, except the reaction is stirred for 40 hours at 95° C. The yield of product is 9.2 g, mp 207°-208° C after recrystallization from ether-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064123
Source datasetuspto-grants-1977_12
ORD IDord-944be1909e354d35bcddfbef83d23670
Source noteuspto-grants-1977_12