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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413474Generated: October 31, 2026

Chloroacetamide → methyl 9H-fluorene-9-carboxylate

https://huagongshe.com/reaction/2413474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetamideHCID 6580—
ReactantSodium HydroxideHCID 14798—
Reactant9-CarboxyfluoreneHCID 74809—
ReactantSodiumHCID 5360545—
ReactantMethyl 2,7-difluoro-9-hydroxy-9H-fluorene-9-carboxylateHCID 14075053—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
Productmethyl 9H-fluorene-9-carboxylateHCID 232396—

Reaction Steps

9H-fluoren-9-carboxylic acid methyl ester (19), which was prepared by refluxing 9H-fluoren-9-carboxylic acid (Aldrich Chemical, Inc.) in HCl/MeOH, (10.0 g, 44.6 mmol) was added to a solution of sodium (1.2 eq, 53.5 mmol, 1.23 g) in 100 mL methanol. After 15 min., 2-chloroacetamide (1.1 eq, 49.1 mmol, 4.59 g) was added and the mixture was allowed to stir at room temperature under nitrogen for two (2) days. The reaction mixture was poured into 400 mL of cold 2.5% w/v aqueous sodium hydroxide and the insoluble material was removed by filtration. The filtrate was chilled and acidified with concentrated hydrochloric acid to precipitate the spiro-succinimide which was collected and air dried to provide 6.7 g (60%). Recrystallization from methanol gave purified (20), 4.28 g (39%). m.p. 237°-239° C. Calc. %C 77.09, %H 4.45, %N 5.62: meas. %C 77.17, %H 4.55, %N 5.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04717725
Source datasetuspto-grants-1988_01
ORD IDord-60b5662776c14fb38ba21a45c2c764a4
Source noteuspto-grants-1988_01