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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038831Generated: October 26, 2026

L-Methionine → HCID 66980706, compound

https://huagongshe.com/reaction/1038831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-MethionineHCID 6137—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantBenzyl 4-cyanopiperidine-1-carboxylateHCID 22028286—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66980706HCID 6698070680.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

LiHMDS (47.6 mL, 47.6 mmol) was added dropwise via syringe to the mixture of benzyl 4-cyanopiperidine-1-carboxylate (8.00 g, 31.8 mmol, [Oakwood]) in THF (50 mL) at about −78° C. and stirred for about 1 h. Met (6.76 g, 47.6 mmol) was added dropwise via syringe at about −78° C. and the mixture was stirred overnight at rt. The solution was cooled to 0° C. and saturated aqueous NH4Cl (200 mL) was added. The mixture was extracted with DCM (3×300 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The sample was deposited onto silica gel and purified by column chromatography eluting with 10:1 pet ether/EtOAc to give benzyl 4-cyano-4-methylpiperidine-1-carboxylate (6.6 g, 74%): LC/MS (Table 2, Method i) Rt=2.03 min; MS m/z: 259 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551981B2
Source datasetuspto-grants-2013_10
ORD IDord-636345933a4e4599a0d0118cb39ab536
Source noteuspto-grants-2013_10