HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258655Generated: October 31, 2026
Hydrochloric Acid → HCID 178460821, compound
https://huagongshe.com/reaction/258655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 70592080 | HCID 70592080 | — |
| Reactant | HCID 178463196 | HCID 178463196 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 178460821 | HCID 178460821 | — |
Reaction Steps
A solution of diphenylmethyl 3-bromomethyl-7β-(2-thienylacetamido)-ceph-3-em-4-carboxylate (11.67g) and 1-ethyltetrazoline-5-thione (2.6 g) in dry tetrahydrofuran (150 ml) was stirred at 0° and a solution of triethylamine (2.8 ml) in tetrahydrofuran (25 ml) was added, dropwise, over 5 minutes. The resulting suspension was stirred for a further 25 minutes, during which time the temperature was allowed to rise to ca. 20°, and was then added, over 5 minutes, to a stirred mixture of 2N-hydrochloric acid (50 ml), water (350 ml), brine (350 ml), and ethyl acetate (600 ml). The organic phase was separated, and washed with 2 N-hydrochloric acid, saturated sodium bicarbonate, water, and brine, and dried and evaporated to a foam (11.71 g). A solution of this foam in benzene (25 ml) was purified by chromatography on kieselgel (200 g), with benzene:ethyl acetate= 5:1 as eluant. Appropriate fractions were combined and the solvents evaporated in vacuo. The residue was dissolved in methylene dichloride, and the solution run into petroleum ether to give the ester as a pale-yellow, amorphous solid (8.585 g, 68%); [ α]D23 - 131° (c 0.97, CHCl3); λmax. (EtOH) 264 nm (ε 7,300), τ (CDCl3) values include 4.12 (7-H, dd, J 5 and 9 Hz.), 5.04 (6-H, d, J 5 Hz.), 5.83 (CH3CH2 --,q, J 7 Hz.), and 8.57 (CH3CH2 --, t, J 7 Hz.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04033950 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-c4601233eae24ce58370411344053052 |
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| Source note | uspto-grants-1977_07 |
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