4-Nitrobenzoyl chloride → HCID 86735367, compound

To a solution of 1 g of compound (IX) in 10 ml of anhydrous pyridine, 2 g of p-nitrobenzoyl chloride were added. After 12 hours at room temperature, the reaction mixture was poured onto ice and the resulting precipitate was washed with water until the water was neutral. The resulting crude 1-p-nitrobenzoate (mixture of α and β anomer) was dried over phosphorus pentoxide for several hours under vacuum, and then dissolved in dry methylene dichloride and saturated at 0° with anhydrous hydrogen chloride. The precipitated p-nitrobenzoic acid was filtered off under anhydrous conditions, and the 1-chloro derivative (II) was obtained in quantitative yield by evaporation of the solvent. Compound (II) can be used for the ensuing condensation reaction without further purification.

1. additionthe reaction mixture was poured onto ice
2. washthe resulting precipitate was washed with water until the water
3. dry with materialThe resulting crude 1-p-nitrobenzoate (mixture of α and β anomer) was dried over phosphorus pentoxide for several hours under vacuum
4. dissolutiondissolved in dry methylene dichloride and saturated at 0° with anhydrous hydrogen chloride
5. filtrationThe precipitated p-nitrobenzoic acid was filtered off under anhydrous conditions

ORD record

ord-128967421f1e4f9dbc824598fa85b1c5

Source dataset

uspto-grants-1978_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04067969