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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257107Generated: October 25, 2026

Salicylamide → o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide

https://huagongshe.com/reaction/257107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylamideHCID 5147—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant3-Hexyl-4-((R)-2-hydroxytridecyl)-2-oxetanone, (3S,4S)-HCID 10428248—
SolventTetrahydrofuranHCID 8028—
Producto-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamideHCID 5413350449.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.1 g of (3S,4S)-3-hexyl-4-[(R)-2-hydroxytridecyl]-2-oxetanone, 1.6 g of triphenylphosphine, 0.825 g of salicylamide and 3 g of molecular sieve (4 Å) were treated with 20 ml of THF and cooled to 0° C. Thereupon, 1.4 g of di-t-butyl azodicarboxylate were added. After warming to room temperature and stirring the reaction mixture was concentrated and the residue was partitioned between methanol/water (70:30) and hexane and extracted with hexane. The hexane phase was dried and concentrated and the residue was chromatographed on silica gel with hexane/ethyl acetate (4:1). There were obtained 0.727 g of o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide, MS: 474 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260310
Source datasetuspto-grants-1993_11
ORD IDord-1ba5356937b74d128baf147e446b59a1
Source noteuspto-grants-1993_11