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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108375Generated: October 31, 2026

Iodoethane → HCID 10704698, compound

https://huagongshe.com/reaction/1108375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexamethylphosphoramideHCID 12679—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-Piperidinone, 3-methyl-1-(phenylmethyl)-HCID 11106446—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10704698HCID 10704698—

Reaction Steps

The reaction of 3-methyl-1-phenylmethyl-2-piperidinone (Meyers A I, Kunnen K B, Still W C (1987) "Conformational effects on the regiochemical metalation of C5-C13 N-benzyl lactams" J. Am. Chem. Soc., 109, 4405-4407.) (3.25 g, 16 mmol) with iodoethane (3.92 g, 25.1 mmol) in the presence of lithium diisopropylamide (prepared by treating diisopropylamine (2.42 g, 24 mmol) with butyllithium in hexanes (2.5 M, 9.2 mL, 22.9 mmol)) in THF (45 mL) and HMPA (2.4 ml,, 13.8 mmol) as described above in the preparation of Example 10, gave 5.90 g of pale yellow colored oil. Column chromatography over silica gel (hexanes-EtOAc, 9:1) afforded the product lactam (2.52 g, 68%) as a colorless viscous liquid. Analytical sample was prepared by bulb-to-bulb distillation (pot temp. 110-115° C. (1 mmHg)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066666
Source datasetuspto-grants-2000_05
ORD IDord-e508cb9fd237467ab303f6f34331014d
Source noteuspto-grants-2000_05