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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379010Generated: October 30, 2026

Thionyl Chloride → HCID 178443552, compound

https://huagongshe.com/reaction/2379010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178443555HCID 178443555—
SolventPotassium CarbonateHCID 11430—
ProductHCID 178443552HCID 178443552—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 1.05 g of 4-(trans-4-heptylcyclohexyl)-N-[(S)-2-hydroxy-1-isopropylethyl)benzamide in 40 ml of acetenitrile was treated dropwise with 0.7 ml of thionyl chloride at 0° C. and while gassing with nitrogen. The reaction mixture was stirred at 0° C. overnight, poured into 100 ml of saturated potassium carbonate solution and then extracted three times with 50 ml of diethyl ether each time. The combined organic phases were washed twice with 50 ml of saturated sodium chloride solution each time, dried over magnesium sulphate, filtered and subsequently concentrated. Chromatography of the residue on silica gel with hexane/ethyl acetate (vol. 2:1) and recrystallization from acetone at -25° C. gave pure (S)-2-[4-(trans-4-heptylcyclohexyl)phenyl]-4-isopropyl-2-oxazoline with m.p. (C-I) 51° C. and cl.p. (S-I) 46° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05360577
Source datasetuspto-grants-1994_11
ORD IDord-4ab1ed5deb7e49fc8b8d469b42aba53b
Source noteuspto-grants-1994_11