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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426802Generated: November 2, 2026

Diisopropyl (S-(R*,R*))-tartrate → HCID 67252928, compound

https://huagongshe.com/reaction/2426802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl (S-(R*,R*))-tartrateHCID 112972—
Reactanttrans-2-Butenal diethyl acetalHCID 6278424—
CatalystBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventBenzeneHCID 241—
ProductHCID 67252928HCID 6725292855.3%

Reaction Steps

A solution of (2E)-1,1-diethoxybut-2-ene (32.20 g, 223.27 mmol), (−)-diisopropyl D-tartrate (64.64 mL, 245.60 mmol) and pyridinium tosylate (2.24 g, 8.93 mmol) in 100 mL benzene was heated to 95° C. to distill off the solvent and EtOH produced. After 7 h at 95° C., the reaction was cooled to rt and concentrated in vacuo. Purification by normal phase chromatography (10->30% EtOAc/hexanes) yielded 35.37 g (55%) of diisopropyl (4S,5S)-2-[(1E)-prop-1-enyl]-1,3-dioxolane-4,5-dicarboxylate as an orange oil. 1H NMR (CDCl3, 400 MHz) 6.03 (m, 1H); 5.86 (m, 2H); 5.12 (m, 2H); 4.71 (d, J=3.84 Hz, 1H); 4.63 (d, J=3.84 Hz, 1H); 1.78 (m, 3H); 1.30 (d, J=6.23 Hz, 12H); LC/MS [M+H]+=287.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968571B2
Source datasetuspto-grants-2011_06
ORD IDord-d4968ab8bfaa4a02847075a3026e2749
Source noteuspto-grants-2011_06