HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Mandelonitrile, (+)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Product | Mandelonitrile, (+)- | HCID 9548674 | — |
Reaction Steps
To a solution of L(+)-tartaric acid derivative shown in Table 1 (2 mmol) in a solvent shown in Table 1 (20 ml), a tetraalkyl titanate shown in Table 1 (2 mmol) was dropwise added and stirred for 30 minutes at room temperature. After evaporating volatile components off in the same manner as in Example 1, a solvent shown in Table 1 (20 ml) was added to the residue and stirred at room temperature to obtain a homogeneous solution. To the resulting solution, trimethylsilylcyanide (218 mg) and then benzaldehyde (212 mg) were added and stirred for 14 hours at room temperature. After the reaction, the reaction mixture was treated in the same manner as in Example 1. The product was analyzed by HPLC. The results are shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05003083 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-4a4c91b670034a519e3a0e0daaf5f25c |
| Source note | uspto-grants-1991_03 |