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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637897Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 15406682, compound

https://huagongshe.com/reaction/1637897

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantL-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
ProductHCID 15406682HCID 15406682—

Reaction Steps

(4S)-N-tert-Butyloxycarbonyl 4-isobutyl-1,3-oxazolidin-5-one (4) was prepared from N-tert-butyloxycarbonyl-(L)-leucine (2.31 g, 10.0 mM) and para-toluenesulfonic acid (30 mg) following general procedure A and obtained as a colourless, slowly solidifying oil after purification by flash column chromatography, using 30% chloroform/petroleum ether as eluant (1.91 g, 79%): [α] D20 +88.5 (c 0.9, CHCl3); IR (CHCl3): 1790, 1720 cm-1 ; 1H NMR (200 MHz, CDCl3): δ 5.48 (d, J=5 Hz, 1H), 5.09 (d, J=5 Hz, 1H), 4.22 (t, J=6 Hz, 1H), 1.43 (s, 9H), 1.23-1.16 (m, 3H), 0.92 (d, J=5 Hz, 3H), 0.90 (d, J=5 Hz, 3H); 13C NMR (50.3 MHz, CDCl3): δ 172.9, 152.2, 81.5, 77.8, 53.2, 39.4, 27.9, 24.2, 22.4,22.2; LRMS (NH3): 244 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043278
Source datasetuspto-grants-2000_03
ORD IDord-1f76208a970a4799968879b8ff78d29b
Source noteuspto-grants-2000_03