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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719623Generated: October 26, 2026

Dimethylformamide → 2-Chloro-5-formyl-N-(tricyclo [3.3.1.13,7]dec-1-ylmethyl)-benzamide

https://huagongshe.com/reaction/719623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-bromo-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)benzamideHCID 7921308—
ReactantHCID 178418306HCID 178418306—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-5-formyl-N-(tricyclo [3.3.1.13,7]dec-1-ylmethyl)-benzamideHCID 12085346—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 5-bromo-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide (3.25 g, Example 1a) in tetrahydrofuran (150 ml) was cooled to −78° C. under a nitrogen atmosphere. A solution of 1.4M methyllithium in diethyl ether (6.1 ml) was added to this solution over 2 min. The mixture was stirred at −78° C. for 10 min, then a 1.7M solution of tert-butyllithium in pentane (10.0 ml) was added dropwise. The mixture was stirred at −78° C. for a further 10 min., then dimethylformamide (1.0 ml) was added. The resulting solution was stirred at −78° C. for 30 min., quenched with saturated aqueous ammonium chloride solution (100 ml) and extracted with ethyl acetate. The combined extracts were dried over sodium sulfate, filtered, and the filtrate concentrated under reduced pressure to give the subtitled compound as a solid (2.76 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132457B2
Source datasetuspto-grants-2006_11
ORD IDord-f0c3c06a624b43f88ab2cc4d336a7458
Source noteuspto-grants-2006_11