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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390193Erstellt: 23. Oktober 2026

2-(Trifluoromethyl)benzylic alcohol → 2-(Trifluoromethyl)benzyl 7-bromo-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate

https://huagongshe.com/de/reaction/390193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Trifluoromethyl)benzylic alcoholHCID 67666—
EduktBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Edukt7-bromospiro[indene-1,4'-piperidin]-3(2H)-oneHCID 58295671—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(Trifluoromethyl)benzyl 7-bromo-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylateHCID 44227079—

Reaktionsschritte

To o-(trifluoromethyl)benzyl alcohol (35 mg, 0.20 mmol) in CH2Cl2 (4 mL) was added was a solution of carbonyl diimidazole (29 mg, 0.18 mmol) in CH2Cl2 (4 mL). The mixture was stirred at rt for 2 h. A 1-mL aliquot of the resulting solution (0.05 mmol) was added to a solution 7-bromospiro[indene-1,4′-piperidin]-3(2H)-one (14.5 mg, 0.05 mmol) in CH2Cl2 (1 mL). The mixture was stirred at rt for 16 h, concentrated, redissolved in MeCN (1 mL) and heated at 60° C. for 2 h. Prep HPLC afforded the title compound. LC-MS Method 1 tR=2.06, min, m/z=484, 482.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383629B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-67ab8ad46ead4b3d99d43255073f14ae
Quellennotizuspto-grants-2013_02