HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 15701917, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 15701914 | HCID 15701914 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 15701917 | HCID 15701917 | — |
Reaction Steps
The title compound was prepared from (S)-(-)-N-1-(1-naphthyl)ethyl-N-trimethylsilylmethylamine by reaction with n-butanol and aqueous formaldehyde following the procedure of Example 2 to give the crude acetal (80% pure) as a pale yellow oil (5.5 g, 82%)δH [CD3)2CO] 0.1 (s, SiMe3), 0.93 (t, J 7 Hz, CH3CH2), 1.2-1.7 (m, CH3CH and (CH2)2), 2.22, 2.45 (AB quartet, J 15 Hz, NCH2Si), 3.25 (t, J 7 Hz, CH2O), 4.22, 4.35 (AB quartet, J 10 Hz, NCH2O), 4.78 (q, J 7 Hz, CH), 7.3-8.5 (m, naphthyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05310911 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-8ce43c4d36a042d2962d15d34578415f |
| Source note | uspto-grants-1994_05 |