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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963266Generated: October 31, 2026

Pentane → tert-Butyl 4-Methoxy-2-(trimethylstannyl)carbanilate

https://huagongshe.com/reaction/963266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantTrimethyltin chlorideHCID 14016—
Reactanttert-Butyl-4-methoxycarbanilateHCID 2741326—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl 4-Methoxy-2-(trimethylstannyl)carbanilateHCID 2210033586.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of t-butyllithium in pentane (1.70M, 148 mL, 251 mmol, 2.50 equiv) was added via cannula to a solution of tert-butyl 4-methoxycarbanilate (22.4 g, 100 mmol, 1 equiv) in ether (500 mL) at -20° C., producing a cloudy yellow solution. After stirring at -20° C. for 5 h, the reaction mixture was cooled to -78° C. and a solution of trimethyltin chloride (50.0 g, 251 mmol, 2.50 equiv) in ether (50 mL) was added via cannula. After the addition, the reaction mixture was warmed to -20° C. and was stirred at that temperature for 30 min, then was stirred in an ice bath for 30 min. The product solution was partitioned between aqueous phosphate buffer solution (pH 7, 0.05M in sodium hydrogen phosphate and 0.05M in potassium dihydrogen phosphate, 600 mL) and ether (400 mL). The aqueous layer was separated and further extracted with ether (2×400 mL). The combined organic layers were dried over sodium sulfate and were concentrated. The product was purified by flash column chromatography (15% ethyl acetate-hexanes) to afford tert-butyl 4-methoxy-2-(trimethylstannyl)carbanilate (7) as a yellow oil (33.3 g, 85%). ##STR19##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763451
Source datasetuspto-grants-1998_06
ORD IDord-1c617a6524e8444cada4ace92f30e0c2
Source noteuspto-grants-1998_06