推薦產品
等級
technical
化驗
≥90% (GC)
折射率
n20/D 1.539 (lit.)
n20/D 1.541
bp
75-77 °C/0.2 mmHg (lit.)
密度
1.22 g/mL at 25 °C (lit.)
官能基
ester
thioether
SMILES 字串
CCOC(=O)C1SCCCS1
InChI
1S/C7H12O2S2/c1-2-9-6(8)7-10-4-3-5-11-7/h7H,2-5H2,1H3
InChI 密鑰
ANEDZEVDORCLPM-UHFFFAOYSA-N
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一般說明
Ethyl 1,3-dithiane-2-carboxylate is an α-keto acid equivalent and bulky equivalent of acetate. It participates in syn-selective aldol reactions. It can be prepared from the reaction of ethyl diethoxyacetate and 1,3-propanedithiol in the presence of BF3/Et2O. Asymmetric oxidation of ethyl 1,3-dithiane-2-carboxylate by Modena protocol has been reported to afford trans bis-sulfoxide in 60% yield. Carbanion from ethyl 1,3-dithiane-2-carboxylate may be employed for the preparation of α-keto esters.
Convenient synthesis of α-keto esters.
The Journal of Organic Chemistry, 37(3), 505-506 (1972)
Aldol condensations of ethyl 1,3-dithiolane-2-carsoxylate and ethyl 1, 3-dithiane-2-carboxylate with chiral aldehydes. Exceptional diastereoface selectivity from two convenient acetate equivalents.
Tetrahedron Letters, 26(25), 2977-2980 (1985)
Phase Transfer Catalysis for Preparation and Alkylation of Ethyl 1,3-Dithiane-2-carboxylate.
Synthetic Communications, 11(4), 343-346 (1981)
Alkylation of the carbanion from methyl bis (ethylthio) acetate with alkyl and aralkyl halides.
The Journal of Organic Chemistry, 41(12), 2228-2229 (1976)
Dianions of glyoxylic acid thioketals: conventent α-keto acid equivalents.
Canadian Journal of Chemistry, 58(7), 716-722 (1980)
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