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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982899Generated: November 1, 2026

Ammonium Chloride → HCID 11659501, compound

https://huagongshe.com/reaction/1982899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67527045HCID 67527045—
ReactantHCID 178448414HCID 178448414—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11659501HCID 1165950135%

Reaction Conditions

Temperature-20 °C

Reaction Steps

(4-Fluorobenzyl)-(4-nitropyridin-3-yl)-carbamic acid tert-butyl ester (5.1 g) prepared in Step 2 was dissolved in anhydrous tetrahydrofuran (100 ml) under a nitrogen atmosphere. 1-Methyl-1-propenyl magnesium bromide (0.5M in tetrahydrofuran solution, 55.0 ml, 65.2 mmol) was added at −78° C. to the solution, which was then stirred for 5 hours at −20° C. 20 ml of 20% ammonium chloride solution was added to the reaction mixture, which was then extracted with ethyl acetate (200 ml) twice. The separated organic layer was dried on anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/methanol=10/1 (v/v)), dissolved in 1 ml of ethyl acetate and then saturated with hydrochloric acid gas. The resulting precipitate was filtered to give the titled compound as a pale yellow solid (2.1 g, 35.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541366B2
Source datasetuspto-grants-2009_06
ORD IDord-74cfddbc8c554fadb9041791e023f1e1
Source noteuspto-grants-2009_06