Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Benzene ethyl acetate | HCID 21583983 | — |
| Reactant | HCID 53967098 | HCID 53967098 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54246851 | HCID 54246851 | — |
Reaction Steps
20 g of 3,7,11,15,19,23,27,31,35,39-decamethyl-6,10,14,18,22,26,30,34,38-tetracontanonaenic acid are dissolved in 100 ml of methylene chloride. To this solution, 6.9 g of N,N-dicyclohexylcarbodiimide are added with cooling at 0° C., and stirred for 1.0 hour. Ammonia gas is blown little by little into this solution during an hour. Stirring for 3.0 hours is performed at room temperature after the end of addition of ammonia. Mother liquor is condensed after filtering off N,N-dicyclohexylurea formed. The residue is subjected to silica gel column chromatography using benzene/ethyl acetate mixture for eluting solvent. The desired product was obtained as an oily substance light yellow in color (yield: 12.3 g). This oily substance was dissolved in 50 ml of acetone and left overnight in a refrigerator. The white crystals deposited were filtered off, dried and thus yielded 8.5 g of desired final product, acid amide derivative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04555365 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-8c461ce6b883472081ca17ec3d5b46da |
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| Source note | uspto-grants-1985_11 |
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