43749
Ethyl 1,3-dithiane-2-carboxylate
technical, ≥90% (GC)
Synonym(s):
Glyoxylic acid ethyl ester trimethylenemercaptal
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About This Item
Empirical Formula (Hill Notation):
C7H12O2S2
CAS Number:
Molecular Weight:
192.30
Beilstein:
1424352
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical
Assay
≥90% (GC)
refractive index
n20/D 1.539 (lit.)
n20/D 1.541
bp
75-77 °C/0.2 mmHg (lit.)
density
1.22 g/mL at 25 °C (lit.)
functional group
ester
SMILES string
CCOC(=O)C1SCCCS1
InChI
1S/C7H12O2S2/c1-2-9-6(8)7-10-4-3-5-11-7/h7H,2-5H2,1H3
InChI key
ANEDZEVDORCLPM-UHFFFAOYSA-N
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General description
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.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
131.0 °F - closed cup
Flash Point(C)
55 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Alkylation of the carbanion from methyl bis (ethylthio) acetate with alkyl and aralkyl halides.
Lerner LM.
The Journal of Organic Chemistry, 41(12), 2228-2229 (1976)
Convenient synthesis of α-keto esters.
Eliel EL and Hartmann AA.
The Journal of Organic Chemistry, 37(3), 505-506 (1972)
Varinder K. Aggarwal et al.
The Journal of organic chemistry, 63(21), 7306-7310 (2001-10-24)
Asymmetric oxidation of a range of 1,3-dithianes was studied using the Kagan protocol [CHP (4 equiv), (+)-DET (2 equiv), Ti(OiPr)(4) (1 equiv), and H(2)O (1 equiv) at -35 degrees C for 48 h]. 1,3-Dithiane itself gave monoxide (30% ee) and
Dianions of glyoxylic acid thioketals: conventent α-keto acid equivalents.
Bates GS and Ramaswamy S.
Canadian Journal of Chemistry, 58(7), 716-722 (1980)
L.A. Flippin et al.
Tetrahedron Letters, 26, 2977-2977 (1985)
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