HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dimethoxybenzene → HCID 13363429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dimethoxybenzene | HCID 9016 | — |
| Reactant | HCID 13363400 | HCID 13363400 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13363429 | HCID 13363429 | — |
Reaction Steps
4-(2',5'-Dimethoxyphenyl)-α,α,1-trimethyl-4-piperidinemethanol was prepared from 1,4-dimethoxybenzene by the procedure described in Example 3 except that acetone was used in place of cyclopentanone in the synthesis of III; m.p. 139°-140°; NMR (in CDCl3): τ 3.0-3.3 (m, 3H); 6.2 (2s, 6H); 6.6-8.5 (m+s, 12H) and 8.9 (broad, 6H). Anal. Calcd. for C17H27NO3 : C, 69.59; H, 9.29; N, 4.77. Found: C, 69.66; H, 9.09; N, 4.66.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04485109 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-1d9d9d66ba054ea083bfcffde47d233c |
| Source note | uspto-grants-1984_11 |