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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979693Generated: October 29, 2026

Oxalyl chloride → HCID 54480172, compound

https://huagongshe.com/reaction/1979693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 54219915HCID 54219915—
ProductHCID 54480172HCID 54480172—

Reaction Steps

Oxalyl chloride (0.72 ml, 8 mM) were reacted with 530 mg (2 mM) of α-methoxyimino-α-(3-methoxy-2-benzothienyl)acetic acid according to the method of Example 6 to give α-methoxyimino-α-(3-methoxy-2-benzothienyl)acetyl chloride. The acid chloride was dissolved in 20 ml of acetone and added dropwise to a cold (0° C.) stirred solution of 428 mg (2 mM) of 7-amino-3-methyl-3-cephem-4-carboxylic acid in 20 ml of acetone and 20 ml of water containing 420 mg (5 mM) of sodium bicarbonate. The reaction mixture was stirred for thirty minutes at 0° C. and then was warmed to 25° C. and stirred for an additional three hours. The reaction mixture was concentrated to a volume of about 20 ml and then was washed with ethyl acetate. The aqueous layer was layered with fresh ethyl acetate and the slurry was diluted with 1N hydrochloric acid to pH 2.4. The organic layer was separated, washed with water, dried, and the solvent was removed by evaporation to give 670 mg (72% yield) of 7-[α-methoxyimino-α-(3-methoxy-2-benzothienyl)acetamido]-3-methyl-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04482553
Source datasetuspto-grants-1984_11
ORD IDord-996fc2858e204c459db00f52327180e2
Source noteuspto-grants-1984_11