Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 5,7,11-Dodecatriyn-1-ol | HCID 93453 | — |
| Solvent | Oxygen | HCID 977 | — |
| Product | HCID 20165401 | HCID 20165401 | — |
Reaction Steps
A mixture of 2 parts cuprous chloride, 12 parts methanol, and 4 parts N,N,N',N'-tetramethylethylenediamine was prepared. To this mixture was added 5,7,11-dodecatriyn-1-ol, produced in Example 22, dissolved in 12 parts methanol over a period of 15 minutes while oxygen was moderately bubbled through the reaction contents. After 1 hour, oxygen flow was stopped and the methanol was distilled leaving a semi-viscous residue. To this was added 100 parts of 3 N hydrochloric acid while stirring, causing product to precipitate. It was collected by filtration, washed once with 25 parts 2 N hydrochloric acid and several times with water. The solid was dissolved in 200 parts xylene and the solution was refrigerated at -8° C. Subsequent crystallization and filtration yielded 6.0 parts of fluffy product, CF4 diol, which turns blue in daylight. The melting point of the material was 101.0° to 104.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04242440 |
|---|
| Source dataset | uspto-grants-1980_12 |
|---|
| ORD ID | ord-020430035c6c49498fe9196ea469d185 |
|---|
| Source note | uspto-grants-1980_12 |
|---|