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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955699Generated: November 1, 2026

Iodoethane → HCID 10704698, compound

https://huagongshe.com/reaction/1955699

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 (2.5M, 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 numberUS05776959
Source datasetuspto-grants-1998_07
ORD IDord-d93e7f378e0b4f0cb6a73c212b12738d
Source noteuspto-grants-1998_07