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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274156Generated: October 31, 2026

Tributylstannane → HCID 71183690, compound

https://huagongshe.com/reaction/2274156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantHCID 86675575HCID 86675575—
SolventBenzeneHCID 241—
ProductHCID 71183690HCID 7118369080%

Reaction Steps

1.15 g (4.36 mmol) of tributyltin hydride, 53.71 mg (0.33 mmol) of α,α′-azoisobutyronitrile and 1.0 g (2.18 mmol) of tert-butyl 3-[benzothiazol-2-yl(imidazole-1-carbothioyloxy)methyl]-piperidine-1-carboxylate were dissolved successively in 10 ml of benzene at room temperature. After 2 min with stirring, a vacuum was applied, and the mixture was degassed for 2 min. This operation was repeated. The reaction mixture was subsequently stirred under reflux for 45 min. Conventional work-up gave 0.58 g of tert-butyl 3-benzothiazol-2-ylmethylpiperidine-1-carboxylate; HPLC/MS (M+H)+=333 as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126952B2
Source datasetuspto-grants-2015_09
ORD IDord-08d5d7cf30e2432894d8992c2a248040
Source noteuspto-grants-2015_09