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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631890Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 2763195, compound

https://huagongshe.com/reaction/631890

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTrifluoroacetic acidHCID 6422—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactanttert-Butyl [(3S)-2-oxooxetan-3-yl]carbamateHCID 2763194—
ProductHCID 2763195HCID 276319581%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of 2 (1.34 mmol) and anhydrous p-toluenesulphonic acid (72 h under vacuum in the presence of P2O5) (1.43 mmol), kept at 0° C. under N2, trifluoroacetic acid (3 mL) was added dropwise in the course of 10 min. The solution was reacted under stirring at 0° C. for 15 min, allowed to reach room temperature, and concentrated at a temperature below 30° C. The oily residue was kept under vacuum for 1 h, and the resulting white solid triturated and washed with dry diethyl ether, then kept under vacuum for 24 h. Yield 81%. Mp and 1H NMR are in accordance with literature (Arnold, et al., 1988).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321743B2
Source datasetuspto-grants-2016_04
ORD IDord-8a443917c8764817a3893f8fe4a38ce2
Source noteuspto-grants-2016_04