HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(1-Formyl-heptyl)-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-(1-Methoxymethylene-heptyl)-benzoic acid methyl ester | HCID 68491171 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Formyl-heptyl)-benzoic acid methyl ester | HCID 86625833 | — |
Reaction Steps
4-(1-Methoxymethylene-heptyl)-benzoic acid methyl ester (3.5 g, 12.68 mmol) is dissolved in tetrahydrofuran (50 mL) and concentrated hydrochloric acid (5 mL) is added. The system is purged of air with nitrogen and heated to reflux for 6 h. The reaction is monitored by HPLC. The reaction is allowed to cool to room temperature and then neutralized with 30% potassium hydroxide solution and bicarbonate. The two phases are separated and the aqueous extracted a second time with diethyl ether. The combined organic extracts are washed with brine, dried over sodium sulfate, and concentrated. The crude material is loaded onto a silica gel column and purified using hexanes/ethyl acetate. MS (ES): 261.2 [M+H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076374B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-eebea886a7004a2e99d91c2deec1147c |
| Source note | uspto-grants-2011_12 |