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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64388Generated: October 29, 2026

1-Butanol → HCID 178448267, compound

https://huagongshe.com/reaction/64388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
Reactant5,6alpha-Epoxicampestane-3beta,17-diolHCID 131737217—
ReactantHCID 178419017HCID 178419017—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 178448267HCID 17844826713%

Reaction Steps

5,6α-epoxicampestane-3β,17-diol (6.8 g, 22.1 mmol, 1 eq) and histamine (4.9 g, 44.1 mmol, 2 eq) were charged in a round-bottomed flask equipped with a magnetic stirrer bar. 1-Butanol (70 ml, 5 vol) was added and the mixture heated to reflux for 40 h. The reaction mixture was cooled at r.t., diluted with methyl-tertbutyl-ether (5 vol) and washed with water (5 vol) and with brine (5 vol). The organic layer was passed through a silica pad (40 g) eluted with methyl-tertbutyl-ether (3 vol) then 10% Methanol/ethyl acetate (60 vol). Fractions of interest were pooled and the solvent was removed under reduced pressure to give (5α-Hydroxy-6β-[2-(1H-imidazol-4-yl)-ethylamino]-campestane-3β,17-diol) as a white solid (5.7 g, 49%). In same conditions, use of ethanol as solvent (40 vol) and Ca(OTf)2 as catalyst gave a 13% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447141B2
Source datasetuspto-grants-2016_09
ORD IDord-ed2c1e2e276f457784b655718ff6f119
Source noteuspto-grants-2016_09