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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
ReactantLithium ChlorideHCID 433294—
ReactantN-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 86653275—
CatalystHCID 178479802HCID 178479802—
SolventDimethylformamideHCID 6228—
ProductN-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 6715528450%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841291B2
Source datasetuspto-grants-2014_09
ORD IDord-457daebb59124a8c80dea501b501c76d
Source noteuspto-grants-2014_09