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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156975Generated: October 31, 2026

Ammonium Chloride → HCID 12859194, compound

https://huagongshe.com/reaction/1156975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesium ChlorideHCID 5360315—
ReactantHCID 12859191HCID 12859191—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12859194HCID 1285919472%

Reaction Conditions

Temperature-70 °C

Reaction Steps

In 7 ml of THF, was dissolved 295 mg of 2-carbomethoxy-3-phenyl-1,3-diazabicyclo[3,3,0]octane. After addition of 138 mg of anhydrous magnesium chloride, the mixture was refluxed for 10 minutes. To the mixture cooled to -70° C., was added dropwise an ether solution of 1.36 equivalents of methylmagnesium bromide. After having been stirred for 15 minutes at -70° C., the reaction mixture was admixed with saturated aqueous ammonium chloride solution and ether and brought to room temperature. The mixture was extracted with ether and the ether layer was dried. The ether layer was freed from the solvent by distillation in vacuo and the residue was purified by alumina column chromatography to obtain 199 mg (72%) of 2-acetyl-3-phenyl-1,3-diazabicyclo[3,3,0]octane. NMR peaks: δ (ppm)=1.5-2.2 (4H, multiplet), 1.9 (3H, singlet), 2.4-3.3 (3H, multiplet), 3.5-3.9 (2H, multiplet), 4.1 (1H, singlet), 6.1-7.1 (5H, multiplet).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04337346
Source datasetuspto-grants-1982_06
ORD IDord-62a8c4f12f5a4b519713ddaec9cbf7d9
Source noteuspto-grants-1982_06