HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Vinylbenzoic acid → HCID 70363320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Vinylbenzoic acid | HCID 14098 | — |
| Reactant | 1-Naphthalenemethanamine, alpha-methyl-, (alphaS)- | HCID 66325 | — |
| Reactant | 4-(Prop-2-en-1-yloxy)benzoic acid | HCID 460690 | — |
| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Product | HCID 70363320 | HCID 70363320 | — |
Reaction Steps
(R)-N-α-Methylbenzyl-4-vinylbenzamide was prepared as above in Example 1 except 2.5 g (0.017 mole) of 4-vinylbenzoic acid and 2.13 g (0.018 mole) of (R)-α-methylbenzylamine (Aldrich) were used rather than the 2.0 g of 4-allyloxybenzoic acid and 2 g of (S)-1-(1-naphthyl)ethylamine in Example 1. The product was recrystallized from absolute ethanol to give 1.85 g (44%) of white crystals; mp 162°-163° C.; [α]D25 -25.49° (c=0.404, CHCl3); IR (KBr): 3390 and 1640 cm-1 ; NMR (δ): 1.64 (3H, d, J=7.4 Hz); 5.32 (1H, q, J=7.4 Hz); 5.44-5.94 (2H, m); 6.48-6.92 (2H, m), 7.24-7.82 (9H, m). Anal. for C17H17NO: Calcd: C, 81.27; H, 6.77. Found: C, 81.24; H, 6.79.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04909935 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-0c06f36a9e694ead8e29591a4bf8fe6a |
| Source note | uspto-grants-1990_03 |