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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67935Generated: October 29, 2026

1,5-Diazabicyclo(5,4,0)undec-5-ene → HCID 20526317, compound

https://huagongshe.com/reaction/67935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-Diazabicyclo(5,4,0)undec-5-eneHCID 314112—
ReactantBenzyl 6-benzyl-3-chloro-3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylateHCID 20526338—
SolventEthyl AcetateHCID 8857—
ProductHCID 20526317HCID 2052631787.1%

Reaction Steps

A solution of benzyl 6-benzyl-3-chloro-3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylate (79) (0.020 g) in ethyl acetate (2 ml) was treated with 1,5-diazabicyclo[5.4.0]undec-5-ene (0.0069 g). It was stirred for 15 mins. at room temperature and then the solution was washed with brine and dried over sodium sulphate. Concentration of the solution gave benzyl 6-benzyl-3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (80) (0.016 g) as a colourless gum; νmax (CHCl3) 2990, 1790, 1725 and 1590 cm-1 ; λmax (ethanol) 308 nm; τ (CDCl3) 2.5-2.9 (10H, m, phenyls), 4.66 and 4.82 (2H, ABq J 12 Hz, OCH2), 5.99 (1H, ddd J 10, 8 and 3 Hz, C5-H), 6.39 (1H, ddd J 9 6 and 3 Hz, C6-H), 6.6-7.2 (4H, m, C4-H2 and C8-H2), 7.20 (2H, q J 71/2 Hz, SCH2) and 8.76 (3H, t J 71/2 Hz, CH3); (M+ at m/e 409.1333 C23H23NO4S requires 409.1348).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04347181
Source datasetuspto-grants-1982_08
ORD IDord-3de51e59fe1a42a3a4faca155d2d6204
Source noteuspto-grants-1982_08