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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79978Erstellt: 24. Oktober 2026

(Dimethyl sulfide)trihydroboron → Ethyl 5-oxa-6-azaspiro[3.4]octane-7-carboxylate

https://huagongshe.com/de/reaction/79978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(Dimethyl sulfide)trihydroboronHCID 12423031—
EduktEthyl 5-oxa-6-azaspiro[3.4]oct-6-ene-7-carboxylateHCID 59611573—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 5-oxa-6-azaspiro[3.4]octane-7-carboxylateHCID 5961153829%

Reaktionsschritte

To a solution of crude 5-oxa-6-aza-spiro[3.4]oct-6-ene-7-carboxylic acid ethyl ester (7.5 g, <40.9 mmol) in tetrahydrofuran (270 mL) at 0° C. was slowly added a solution of borane-dimethyl sulfide complex (10 M in THF, 16.4 mL, 164 mmol). The reaction was allowed to warm to room temperature overnight then recooled to 0° C., and quenched by the careful addition of water. The mixture was diluted with ethyl acetate, washed with water and brine, dried (MgSO4), and concentrated to yield a large amount of white solids. These solids were thoroughly triturated three times with dichloromethane (150 mL). The combined dichloromethane washings were concentrated and the resulting oil was purified by flash chromatography to yield 5-oxa-6-aza-spiro[3.4]octane-7-carboxylic acid ethyl ester (1.08 g, 29% over 2 steps). 1H-NMR: 400 MHz, (CDCl3) δ: 8.01-7.95 (br, 1H), 4.39-4.28 (m, 2H), 4.18-4.10 (m, 1H), 2.80-2.75 (m, 1H), 2.62-2.49 (m, 2H), 2.37-2.29 (m, 1H), 2.25-2.17 (m, 1H), 2.13-1.95 (m, 1H), 1.88-1.79 (m, 1H), 1.68-1.56 (m, 1H), 1.34 (t, J=7.1 Hz, 3H) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841278B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-1d532bace8a64ce49db4c847de4d6ada
Quellennotizuspto-grants-2014_09