HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 3-(1-Adamantyl)-4,5-methylenedioxybromobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1-Adamantanol | HCID 64152 | — |
| Reactant | 1-Bromo-3,4-(methylenedioxy)benzene | HCID 75831 | — |
| Product | 3-(1-Adamantyl)-4,5-methylenedioxybromobenzene | HCID 19429702 | 86% |
Reaction Steps
A mixture of 4-bromo-1,2-methylenedioxybenzene (2.00 g, 9.95 mmol), 1-adamantanol (1.52 g, 9.95 mmol), and MeSO3H (5 mL) was stirred for 1 h. The resulting solution was quenched with H2O (40 mL) and extracted with EtOAc (110 mL). The extract was washed with 0.5 N NaOH, sat. NaHCO3, and brine and dried. The residue obtained on concentration was purified on silica gel (hexane) to give 2.86 g (86%) of 4-(1-adamantyl)-6-bromobenzo[1,3]dioxole as a white solid, mp 135-136° C. IR 2901, 2843, 1435, 1189 cm−1; 1H NMR δ (CDCl3) 1.76 (bs, 6H, AdCH2), 1.98 (bs, 6H, AdCH2), 2.06 (bs, 3H, AdCH), 5.93 (s, 2H, CH2), 6.84 (s, 1H, 7-ArH), 6.86 ppm (s, 1H, 5-ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096544B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-836acf3b6c2944deb3b75e09dcf11d1e |
| Source note | uspto-grants-2015_08 |