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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398136Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 131710753, compound

https://huagongshe.com/reaction/2398136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiethyl EtherHCID 3283—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131710752HCID 131710752—
SolventAnisoleHCID 7519—
ProductHCID 131710753HCID 131710753—

Reaction Steps

Trifluoroacetic acid (8 ml.) was added to a solution of the above ester (1.387 g.) in anisole (2 ml). at 20°. After 5 minutes the solution was concentrated under reduced pressure and the residue was dissolved in ethyl acetate. The solvent was evaporated and again the residue was dissolved in ethyl acetate. The solution was washed with water and then extracted with sodium bicarbonate solution. The combined extracts were washed with ethyl acetate, then taken to ph 1.9 with concentrated hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and brine, dried and concentrated under reduced pressure to give a foam. Trituration with ether gave the title compound as a buff solid (0.50 g.), [α]D - 84° (c 1, DMSO), λmax. (pH 6 buffer) 271.5 nm (ε 17,600), νmax. (Nujol) include 3250 (NH), 1780 (β-lactam), 2600 + 1710 (CO2H), and 1674 + 1548 cm.-1 (CONH), τ values (DMSO-d6) 0.24 (doublet, J 8 Hz; NH) 2.37 and 2.82 (thienyl protons) 4.12 (double doublet, J 5 and 8 Hz; C-7H), 4.76 (doublet, J 5 Hz; C-6H), 5.40 and 5.75 (2 doublets, branches of quartet, J 13 Hz; C-3 Ch2), 6.13 + 6.40 (2 doublets, branches of quartet, J 18 Hz; C-2 CH2) and 7.29 (singlet; CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024134
Source datasetuspto-grants-1977_05
ORD IDord-229460af41ce4d668bdac99a06401289
Source noteuspto-grants-1977_05