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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282992Generated: October 31, 2026

Trifluoroacetic acid → HCID 131710418, compound

https://huagongshe.com/reaction/1282992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131710419HCID 131710419—
SolventAnisoleHCID 7519—
ProductHCID 131710418HCID 131710418—

Reaction Steps

A solution of diphenylmethyl 3-(2-cyanoethyl)-7β-(2-thienylacetamido)ceph-3-em-4-carboxylate (1g.) in anisole (1 ml.) was treated with trifluoroacetic acid (4 ml.). After 5 minutes at 23° the solvents were removed in vacuo and the residue was partitioned between ethyl acetate and dilute aqueous sodium bicarbonate solution. The alkaline phase was washed thoroughly with ethyl acetate, then taken to pH2 with 2N-hydrochloric acid. The acidic mixture was extracted with ethyl acetate and the organic extracts washed with brine, and dried and evaporated in vacuo. The residual gum was dissolved in ethyl acetate and the solution run into petroleum ether to give, after filtration and drying, the title acid (567 mg., 82%) as an amorphous solid, m.p. ca 105° (decomp.) [α]D22 + 102° (C 0.75, 1% NaHCO3), λinflex. (0.1 M-pH 6 phosphate buffer) 260 nm. (ε 7,290), νmax. (Nujol) 3300 (NH), 3675 to 2400 (bonded OH), 2210 and 2250 (CN), 1775 (β-lactam), 1715 (CO2H), and 1665 and 1530 cm.-1 (CONH), τ (D2O with NaHCO3) 4.43 (C(7) --H, d, J 4.5 Hz), 4.95 (C(6) --H, d, J 4.5 Hz.), 6.13 (CH2CONH), 6.42 and 6.82 (C(2), AB-q, J 18 Hz.), and 7.1 to 7.6 (CH2CH2CN, ABCD-complex) (Found: C, 50.7; H, 4.0; N, 10.7; S, 16.0; C16H15N3O4S2 requires C, 50.9; H, 4.0; N, 11.1; S, 17.0%), Rf 0.28 (System C) and Rf 0.6 (System B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03974152
Source datasetuspto-grants-1976_08
ORD IDord-5f9ddd72a92b4dc8a1d3524041728038
Source noteuspto-grants-1976_08