Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052335Generated: October 27, 2026

Methanol → Stearyl anthranilate

https://huagongshe.com/reaction/1052335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantStearyl AlcoholHCID 8221—
ReactantIsatoic AnhydrideHCID 8359—
ReactantDabcoHCID 9237—
SolventDimethylformamideHCID 6228—
ProductStearyl anthranilateHCID 1208128885%

Reaction Conditions

Temperature100 °C

Reaction Steps

was prepared as described in Example II of U.S. Pat. No. 6,590,082, which is hereby incorporated by reference herein in its entirety. A mixture of octadecanol (270 grams, 1.0 mol; obtained from Sigma-Aldrich Co., Milwaukee, Wis.), isatoic anhydride (24 grams, 1.5 mol; obtained from Sigma-Aldrich Co.), and 1,4-diazabicyclo[2.2.2]octane (56 grams, 0.50 mol; obtained from Sigma-Aldrich Co.) in 1,000 milliliters of dimethylformamide was stirred and heated to 100° C. in a 4 liter beaker. Vigorous gas evolution occurred. After 10 minutes, the resultant brown solution was heated to 150° C. for 15 minutes. The reaction mixture was then cooled to 50° C. and vigorously stirred while 3,000 milliliters of methanol was added. The resultant suspension was stirred for 0.5 hour followed by vacuum filtration. The solid thus obtained was washed in the filter funnel with 4×300 milliliter portions of methanol and then dried in air to give the product stearyl anthranilate as white power (330.5 grams, 85 percent yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388320B2
Source datasetuspto-grants-2016_07
ORD IDord-d46681767d7f4d8b81c871dd70eec4b1
Source noteuspto-grants-2016_07