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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504937Generated: November 1, 2026

Triethylamine → 6-Chloro-inden-1-one

https://huagongshe.com/reaction/1504937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 20463006HCID 20463006—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-inden-1-oneHCID 8667491526.9%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

13.4 kg 3-Bromo-6-chloro-indan-1-one (A; for references on this material, see: Bøgesø EP 35363 A1 19810909 and Kehler, Juhl, Püschl, WO 2008025361; each herein incorporated by reference in its entirety) was dissolved in tetrahydrofuran (170.8 L), and the solution was cooled to 0-5° C. (Scheme 9). Triethylamine (9.1 L) was added over 0.5 h. The mixture was stirred at 0-5° C. for 5 hours before an additional portion of triethylamine (2.48 L) was added over 0.5 hour, and stirring was continued for 2 hours. The mixture was filtered, and the filtrate was concentrated to 30 L before n-heptane (102 L) was added. The volume was reduced to 60 L. More n-heptane (203 L) was added, and the mixture was stirred for 1 hour. Silica gel (17.2 kg) was added. The mixture was filtered, and the residual solid was washed with n-heptane (100 L). The combined filtrates were concentrated to 30 L and stirred at 0-5° C. for 1 hour. The mixture was centrifuged, and the residual solid was dried to afford 6-chloro-inden-1-one (compound B; 2.42 kg) sufficiently pure for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216961B2
Source datasetuspto-grants-2015_12
ORD IDord-38dc9d90c7cf492ab872977935edbd0b
Source noteuspto-grants-2015_12