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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955302Generated: October 31, 2026

Methanol → HCID 22829433, compound

https://huagongshe.com/reaction/1955302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSanglifehrin AHCID 5388925—
ProductHCID 22829433HCID 22829433—

Reaction Steps

To a stirred, cooled (0° C.) solution of 20 mg (18.3 μmol) of Sanglifehrin A in 0.5 mL of methanol is added one crystal of paratoluenesulfonic acid monohydrate. The resulting yellow solution is stirred for one hour and the reaction is quenched with saturated aqueous sodium bicarbonate solution. The resulting mixture is extracted twice with ethyl acetate. The organic solution is washed twice with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel (95:5 methyl-tert.-butyl ether:methanol) to yield Sanglifehrin C as a white amorphous powder. The latter consisted of a 4:1 mixture of Sanglifehrin C and its C53 epimer, Sanglifehrin C having the (S) configuration as depicted below (R=Me). ##STR53##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124453
Source datasetuspto-grants-2000_09
ORD IDord-b2187ee870934d4eb9930fc54d8ab738
Source noteuspto-grants-2000_09