In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Photolysis of benzyl aminoacetates, published in 1974, which mentions a compound: 3235-67-4, mainly applied to benzyl aminoacetate photolysis singlet; pyrrolidinylacetate benzyl photolysis singlet; piperidinoacetate benzyl photolysis singlet; morpholinoacetate benzyl photolysis singlet, Synthetic Route of C7H13NO2.
The photolysis (Hg lamp, under N at room temperature for 48 hr) of RCH2CO2CH2Ph, (R = Et2N, 1-pyrrolidinyl, piperidino, or morpholino), 0.1M in C6H6, yielded R(CH2)2Ph, RCH2CO2H, AcOCH2Ph, Me2C6H4, Ph(CH2)2Ph, and PhCH2OH. The addition of piperylene, a triplet quencher, had very little effect. Yields in EtOH and MeCN are also tabulated; conversions were 79-100%. Solvent quenching effects support a singlet path for this photoreaction.
The article 《Photolysis of benzyl aminoacetates》 also mentions many details about this compound(3235-67-4)Synthetic Route of C7H13NO2, you can pay attention to it, because details determine success or failure
Reference:
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem