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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683174Generated: October 27, 2026

HCID 10549387, compound → benzhydryl (E)-(2S,3S,5R)-3-(3-hydroxy-propenyl)-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate

https://huagongshe.com/reaction/1683174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10549387HCID 10549387—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
Productbenzhydryl (E)-(2S,3S,5R)-3-(3-hydroxy-propenyl)-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylateHCID 10645194—

Reaction Conditions

Temperature0 °C

Reaction Steps

5.80 g (14.2 mmol) of benzhydryl (E)-(2S,3S,5R)-3-(2-formyl-vinyl)-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2carboxylate were dissolved in 240 ml of toluene under argon and is cooled to 0° C. Then, 14.2 ml (21.3 mmol) of a 20% diisobutylaluminium hydride solution (in toluene) were added dropwise and the cooling bath is removed. The reaction mixture was stirred at room temperature for 6 hours, poured into 150 ml of saturated ammonium chloride solution and extracted three times with 200 ml of methylene chloride each time. The combined organic extracts were washed once with 300 ml of water as well as saturated sodium chloride solution, dried over magnesium sulfate, filtered and freed from solvent on a rotary evaporator. The residual yellow oil was chromatographed over silica gel (particle size 0.040-0.063 mm) with ethyl acetate:n-hexane (9:16) as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637579
Source datasetuspto-grants-1997_06
ORD IDord-fd787c0862ea4562a847cca83830d261
Source noteuspto-grants-1997_06