HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium cyanoborohydride → HCID 22485646, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 73988966 | HCID 73988966 | — |
| Product | HCID 22485646 | HCID 22485646 | — |
Reaction Steps
Reduction of 3-fluoro-4-methyl-benzaldehyde O-methyloxime with sodium cyanoborohydride as described in the preparation of compound 1-B gave the title hydroxylamine as a clear oil after chromatography on silica gel (elution hexane-ethyl acetate 8: 2) (57% yield). 1HNMR 400 MHz (CDCl3) δ (ppm): 2.25 (3H, broad s, CH3), 3.50 (3H, s, OCH3), 3.99 (2H, broad s, NCH2), 5.71 (1H, broad, NH), 7.01 (2H, m, aromatics), 7.13 (1H, m, aromatic). The hydrochloride salt was obtained as a white solid: mp 140-142° C. Anal. calcd for C9H12FNO—HCl: C, 52.56; H, 6.37; N, 6.81. Found: C, 52.63; H, 6.30; N, 6.78.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890942B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-d2c45d925eee4e158ec4a5a372f63fc5 |
| Source note | uspto-grants-2005_05 |