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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197594Generated: November 2, 2026

Methyl iodide → HCID 67499019, compound

https://huagongshe.com/reaction/2197594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-(tert-Butyldimethylsilyloxy)cyclohexanoneHCID 10609430—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67499019HCID 6749901986%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 5.0 L round bottom flask containing 4-(tert-butyldimethylsilyloxy)cyclohexanone (7.03 g, 30.8 mmol) (Aldrich) was added THF (100 mL) and the reaction was cooled to −78° C. To the reaction mixture was added lithium bis(trimethylsilyl)amide (33.9 ml, 33.9 mmol) (Aldrich) and the reaction mixture was stirred for 30 minutes followed by the addition of iodomethane (2.309 ml, 36.9 mmol). The reaction mixture was stirred for 30 minutes at −78° C. and 2 hours at room temperature, quenched with saturated NH4Cl, extracted with EtOAc (200 mL), dried (NaSO4), filtered, and concentrated in vacuo. The residue was purified on SiO2 and eluted with 0-20% ethyl acetate/hexane to give a white solid (6.40 g) in 86% yield. 1H NMR (300 MHz, CDCl3) δ ppm 4.19-4.07 (m, 1H), 2.98-2.72 (m, 1H), 2.50-1.99 (m, 2H), 1.91-1.64 (m, 2H), 1.62-1.44 (m, 1H), 1.15 (dt, J=4.4, 6.8, 1H), 1.07-0.99 (m, 3H), 0.95-0.85 (m, 9H), 0.11 (d, J=1.6, 6H). MS (DCI+) M/Z 243.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338603B2
Source datasetuspto-grants-2012_12
ORD IDord-429e94238bf94dcaa5883f95ed1b6653
Source noteuspto-grants-2012_12