Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cetyl Alcohol | HCID 2682 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Hexadecyl Cyanoacetate | HCID 10049542 | — |
Reaction Steps
The esterification reaction of hexadecanol was carried out under an inert atmosphere (Argon). To a solution of cyanoacetic acid (7.4853 g) and of hexadecanol (10.6674 g) in 50 ml of anhydrous dichloromethane and 5 ml of ethyl acetate, 50 ml of anhydrous dichloromethane containing 9.9864 g of dicyclohexylcarbodiimide (DCC) and 50 mg of 4-(dimethylamino)pyridine (DMAP) were added. The reaction mixture was stirred for 24 hours at room temperature. Then 50 ml of anhydrous hexane were added. The formed solid residue was separated by filtration under vacuum and washed with n-hexane (70 ml). The filtrate was concentrated under reduced pressure until obtaining an amorphous yellow solid, subsequently purified by flash chromatography (ligroin/ethyl acetate 9/1 v/v), yielding 14 g of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580820B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-1dbd6271138d44ce99e84b725563ac0c |
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| Source note | uspto-grants-2013_11 |
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