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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165392Generated: November 1, 2026

4-Vinylbenzoic acid → HCID 70363320, compound

https://huagongshe.com/reaction/1165392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Vinylbenzoic acidHCID 14098—
Reactant1-Naphthalenemethanamine, alpha-methyl-, (alphaS)-HCID 66325—
Reactant4-(Prop-2-en-1-yloxy)benzoic acidHCID 460690—
Reactant1-Phenethylamine, (+)-HCID 643189—
ProductHCID 70363320HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04909935
Source datasetuspto-grants-1990_03
ORD IDord-0c06f36a9e694ead8e29591a4bf8fe6a
Source noteuspto-grants-1990_03