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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132102Generated: October 30, 2026

Methanol → HCID 59733775, compound

https://huagongshe.com/reaction/132102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-(3-Tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acidHCID 59733731—
SolventTolueneHCID 1140—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 59733775HCID 597337752.4%

Reaction Steps

Diphenylphosphoryl azide (0.53 mL, 2.46 mmol) was added to a solution of 1-(3-tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid (554 mg, 2.03 mmol) and triethylamine (0.43 mL, 3.08 mmol) in toluene (4 mL). After stirring at ambient temperature for 18 h, the solution was placed into a preheated oil bath at 80° C. Bubbling was observed. After stirring for 1 h at 80° C., the bubbling had ceased and the solution was cooled to ambient temperature. 10% aqueous hydrochloric acid was added and stirred vigorously for 3 h. The aqueous layer was made alkaline with aqueous 3 N NaOH and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was flash chromatographed with 99:1:0.1, 49:1:0.1, 24:1:0.1, and 23:2:0.2 methylene chloride:methanol:concentrated ammonium hydroxide as the eluant to yield 12 mg (2% yield) of 1-(3-tert-butyl-phenyl)-3-methylene-cyclohexylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07385085B2
Source datasetuspto-grants-2008_06
ORD IDord-0ba0571fd228428cbe2b7f0195beb714
Source noteuspto-grants-2008_06