HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717077Generated: October 30, 2026
4-Cyanobenzaldehyde → HCID 123820452, compound
https://huagongshe.com/reaction/717077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | N,N-dimethylformamide methanol | HCID 21901440 | — |
| Reactant | HCID 131734155 | HCID 131734155 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 123820452 | HCID 123820452 | 87.2% |
Reaction Steps
To a stirred solution of 4-formylbenzonitrile (68 mg, 0.51 mmol) and 3-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-azetidine hydrochloride (188 mg, 0.51 mmol) in 1:1 MeOH/DMF (26 mL) was added acetic acid (catalytic). The reaction mixture was stirred under N2 at 0° C. for 1 h. Sodium cyanoborohydride (1M in THF, 0.6 mL, 0.57 mmol) was added and the reaction mixture stirred at RT, under N2 for 18 h. The reaction mixture was concentrated in vacuo, the residue suspended in H2O (10 mL), washed with CH2Cl2 (2×10 mL) and the solution passed through a phase separation cartridge. The combined organic layers were concentrated in vacuo and the crude residue purified by silica gel chromatography eluting with 100% isohexane and increasing the polarity 100% EtOAc to afford 4-[3-(tert-butyl-diphenyl-silanyloxy)-3-methyl-azetidin-1-ylmethyl]-benzonitrile as a colourless oil (196 mg, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09193689B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-12781841910b462dba066ba7975c83f4 |
|---|
| Source note | uspto-grants-2015_11 |
|---|