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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807685Generated: October 30, 2026

Methane → HCID 58092731, compound

https://huagongshe.com/reaction/1807685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantTolueneHCID 1140—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 58092702HCID 58092702—
SolventTrimethylaluminumHCID 16682925—
ProductHCID 58092731HCID 58092731—

Reaction Steps

Trimethylaluminum in toluene (2 M, 2.89 mmol) was added dropwise to a mixture of NH4Cl (2.89 mmol) in toluene (3 mL) at 0° C. with the formation of methane gas. The reaction mixture was allowed to warm to rt, stirred for a further 15 min and then slowly treated with a solution of (2S,3S)-3-morpholin-4-ylmethyl-1-((S)-1-phenyl-ethyl)-pyrrolidine-2-carboxylic acid methyl ester (Stage 37.3) (1.444 mmol) in toluene (9 mL). Additional reagent prepared from NH4Cl (2.89 mmol) in toluene (2 mL) and trimethylaluminum in toluene (2 M, 2.89 mmol) at 0° C. was added after 18 h. After stirring for 60 h, the mixture was cooled to 0° C., quenched with 1M HCl and then washed with CH2Cl2 (3×). The aqueous phase was basified with a 1:1 saturated solution of NaHCO3/saturated solution of Rochelle's salt and extracted with THF (10×). The combined organic layers were dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography to afford the title compound as a yellow oil. HPLC: tR=2.18 min (method G); ESI-MS: [M+H]+ 318.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357707B2
Source datasetuspto-grants-2013_01
ORD IDord-32098a0894b34c5781052e38faecae14
Source noteuspto-grants-2013_01