HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-(Bromomethyl)adamantane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol | HCID 64556 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Bromomethyl)adamantane | HCID 1416304 | — |
Reaction Steps
To 1-Hydroxymethyladamantane (366 gm.) and triphenylphosphine (598 gm.) in 1600 ml. dimethylformamide was added a solution of 366 gm. bromine in 800 ml. dimethylformamide over a 5 hour period. The mixtue was left overnight at room temperature and then distilled (under aspirator) to remove solvent and product. The distillate was poured into 8 liters of water and filtered. The solid was dissolved in petroleum ether (30°-60°), washed with K2CO3 solution, then with water, dried, and concentrated to dryness. The residue recrystallized from 2.5 liters methanol gave 426.6 gm., m.p. 43°-4°. (1st crop plus additional crops obtained on concentration of the mother liquors.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04100170 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-64b0b6bcbf104e7fae646bf53a3ffc8d |
| Source note | uspto-grants-1978_07 |