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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462440Generated: October 30, 2026

Acetic Anhydride → HCID 70477487, compound

https://huagongshe.com/reaction/462440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 12804575HCID 12804575—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 70477487HCID 70477487—

Reaction Steps

Methyl 2β-ethoxy-3α-hydroxy-11α-(3-methylbutylamino)-5α-androstane-17β-carboxylate (464 mg) in chloroform containing dry PTSA (344 mg) was stirred for 20 min, then treated with acetic anhydride (1.0 ml) and the mixture left for 3 h. The reaction mixture was diluted with ethanol and evaporated to give an oil. This was dissolved in ethyl acetate, washed with dilute ammonia solution (2×), water (1×), dried and evaporated to give an oil. This was purified by preparative t.l.c. in CHCl3 /MeOH (20:1) to give the title compound as an oil (415 mg), [α]D +27.9°, νmax 1725 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515786
Source datasetuspto-grants-1985_05
ORD IDord-95734e5f188845df98d6a2255b0ac783
Source noteuspto-grants-1985_05