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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437785Generated: October 30, 2026

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

https://huagongshe.com/reaction/437785

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 numberUS04032537
Source datasetuspto-grants-1977_06
ORD IDord-034e53d58225437098f6bb7c5323e85d
Source noteuspto-grants-1977_06