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Synlett 2023; 34(20): 2447-2450
DOI: 10.1055/a-2088-9219
DOI: 10.1055/a-2088-9219
cluster
Special Issue Dedicated to Prof. Hisashi Yamamoto
Enantioselective Bromination of Silyl Enol Ethers with Chiral Pentacarboxycyclopentadienyl Bromide
This work is supported by the Natural Science Foundation of Beijing Municipality (2202040).
Dedicated to Professor Hisashi Yamamoto on the occasion of his 80th birthday
Abstract
Chiral pentacarboxycyclopentadienyl bromide reagents were synthesized to accomplish enantioselective bromination of silyl enol ethers to give corresponding α-bromoketone products in good yields and up to 77% ee. A catalytic version of this reaction was also demonstrated through the combination of Lewis acid activators and diethyl 2,2-dibromomalonate as stoichiometric achiral bromine source.
Key words
enantioselectivity - asymmetric synthesis - bromine - silyl enol ethers - α-bromoketones - chiral pentacarboxycyclopentadienyl bromideSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2088-9219. Experimental procedures, NMR spectra and HPLC traces are included.
- Supporting Information
Publikationsverlauf
Eingereicht: 17. April 2023
Angenommen nach Revision: 08. Mai 2023
Accepted Manuscript online:
08. Mai 2023
Artikel online veröffentlicht:
14. Juni 2023
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- 17 Typical Procedure for Synthesizing Product 3a To a solution of PCCP-Br 1a (88 mg, 0.083 mmol, 1.0 equiv) in dry DCM (1.5 mL) was added dropwise silyl enol ether (0.1 mmol, 1.2 equiv) at –78 °C. After 22 h, the reaction was quenched by the addition of saturated aqueous NaHCO3 (2 mL) and then extracted with dichloromethane (3 × 2 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography (petroleum ether/ethyl acetate, 175:1 to 20:1) on silica gel to give 18.1 mg of 3a as colorless liquid (97% yield). The enantioselectivity was 69% ee, [α]D 25 +23.2 (c 0.19, CH2Cl2). HPLC conditions: Chiralpak AS-H column [hexanes/2-propanol = 98:2, flow rate = 1.0 mL/min), λ = 254 nm, t R (major) = 9.0 min, t R (minor) = 10.8 min. 1H NMR (400 MHz, CDCl3): δ = 8.09 (d, J = 7.7 Hz, 1 H), 7.54–7.50 (m, 1 H), 7.35 (t, J = 7.6 Hz, 1 H), 7.28 (d, J = 7.7 Hz, 1 H), 4,73 (t, J = 4.3 Hz, 1 H), 3.35–3.27 (m, 1 H), 2.92 (td, J = 17.2, 4.6 Hz, 1 H), 2.57–2.42 (m, 2 H) ppm. 13C NMR (101 MHz, CDCl3): δ = 190.5, 142.9, 134.1, 129.9, 128.7, 128.6, 127.1, 50.4, 31.9, 26.1 ppm.