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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566890Generated: November 1, 2026

Pyridine → HCID 54278690, compound

https://huagongshe.com/reaction/566890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 54342988HCID 54342988—
SolventWaterHCID 962—
ProductHCID 54278690HCID 54278690—

Reaction Conditions

Temperature4 °C

Reaction Steps

iv)—A solution of the aldehyde (12.3 g) mentioned above in dry pyridine (150 ml) was cooled to 4° C. Benzoyl chloride (8 ml) was added in 5 min. and the reaction mixture was stirred for 1.5 h at room temperature. Then it was poured into water (2 l) and the resulting mixture was stirred overnight. The product was extracted into dichloromethane and the combined organic phases were concentrated under reduced pressure to give (3β,5α,20R)-3-(benzoyloxy)-4,4,20-trimethylpregna-8,14-diene-21-carboxaldehyde (16.1 g). The product was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177420B1
Source datasetuspto-grants-2001_01
ORD IDord-253a17a007a54d07b327bbadce7e74ee
Source noteuspto-grants-2001_01