HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565245Generated: October 29, 2026
Sodium Chloride → HCID 70235568, compound
https://huagongshe.com/reaction/565245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 70214614 | HCID 70214614 | — |
| Catalyst | Triphenylphosphine palladium dichloride | HCID 13169693 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70235568 | HCID 70235568 | 54.2% |
Reaction Steps
To a solution of (3R,4S)-1-(2-tetrahydropyranyloxy)-3-((2E)-3-tributylstannyl-2-propene-1-yl)-4-methylazetidin-2-one (400 mg, 0.78 mmol) in 1 mL of dimethylformamide is added 2-bromothiophene (152 mg, 0.93 mmol) and triphenyphosphine palladium (II) dichloride (27 mg, 0.04 mmol). The resulting solution is heated at 80° C. for 2 h, then 0.5 mL ammonium hydroxide is added. The reaction mixture is poured into saturated sodium chloride solution (20 mL) and extracted with 1:1 ethyl acetate/hexane (50 mL). The combined organic layers were dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and purified by silica gel chromatography (elution with 3:1 hexanes-ethyl acetate) to provide (3R,4S)-1-(2-tetrahydropyranyloxy)-3-((2E)-3-(thiophene-2-yl)-2-propene-1-yl)-4-methylazetidin-2-one as an oil (130 mg, 54% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172064B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-69ec5d239fd84559988698d8bc6336a5 |
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| Source note | uspto-grants-2001_01 |
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