HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77323Generated: October 26, 2026
Tetramethyltin → N-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl ester
https://huagongshe.com/reaction/77323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetramethyltin | HCID 11661 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester | HCID 86653275 | — |
| Catalyst | HCID 178479802 | HCID 178479802 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl ester | HCID 67155284 | 50% |
Reaction Steps
To a solution of N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (1.1 g, 1.89 mmol) in N,N-dimethylformamide (20 mL) is added lithium chloride (0.40 g, 9.5 mmol), tetramethyl tin (0.525 mL, 3.79 mmol), and bistriphenylphosphino palladium dichloride (0.066 g, 0.095 mmol). The reaction is heated to 80° C. for 16 h. The reaction is allowed to cool to ambient temperature and filtered through Celite. The filtrate is poured over water and extracted three times with dichloromethane. The combined organic extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by column chromatography (4% hexanes-ethyl acetate) to afford the title compound as a white solid (0.41 g, 50% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841291B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-457daebb59124a8c80dea501b501c76d |
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| Source note | uspto-grants-2014_09 |
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