HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[(4-tert-butylphenyl)methylidene]hydroxylamine → [4-(4-tert-Butyl-benzylideneaminooxymethyl)-phenyl]-acetic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[(4-tert-butylphenyl)methylidene]hydroxylamine | HCID 1275951 | — |
| Reactant | 4-(Bromomethyl)phenylacetic acid | HCID 4519056 | — |
| Product | [4-(4-tert-Butyl-benzylideneaminooxymethyl)-phenyl]-acetic Acid | HCID 72825088 | — |
Reaction Steps
The title compound was prepared as a white solid (0.193 g, 41%) from 4-tert-butyl-benzaldehyde oxime and 4-bromomethyl-phenyl-acetic acid using a procedure similar to example 2. mp=93.3-96.2° C.; mass spectrum (−APCI, M−H) m/z 324. 1H NMR (400 MHz, DMSO-d6); δ 12.30 (bs, 1H), 8.23 (s, 1H), 7.52 (d, 2H), 7.42 (d, 2H), 7.33 (d, 2H), 7.24 (d, 2H), 5.10 (s, 2H), 3.55 (s, 2H), 1.25 (s, 9h). Elemental analysis: Calcd. for C20H23NO3: C, 73.82; H, 7.12; N, 4.30, Found: C, 73.15; H, 7.14; N, 4.01.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07420083B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-65230aef10034faebeebfeedd7ed77b1 |
| Source note | uspto-grants-2008_09 |