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
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 10549387 | HCID 10549387 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | benzhydryl (E)-(2S,3S,5R)-3-(3-hydroxy-propenyl)-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate | HCID 10645194 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05637579 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-fd787c0862ea4562a847cca83830d261 |
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| Source note | uspto-grants-1997_06 |
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