Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 18673386 | HCID 18673386 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18673380 | HCID 18673380 | — |
Reaction Steps
3.85 ml of a 30% solution of sodium methoxide in methanol were added dropwise to a solution of 742 μl of thioglycolic acid in 8 ml of methanol, under an inert atmosphere. The mixture was maintained under stirring for 30 min and then a solution of 2 g of 1-chloro-2,5-dodecadiyne in 20 ml of methanol was added under an inert atmosphere. The mixture was maintained under stirring for 15 hours at room temperature and then the reaction medium was poured over 100 ml of acid water (98 ml of water+2 ml concentrated H2SO4) and then extracted 3 times with ethyl ether. The combined organic phases were washed 3 times with water and then with a saturated aqueous solution of NaCl before being dried (Na2SO4), filtered and concentrated under vacuum in a rotary evaporator. The oily residue obtained crystallized at cold temperature. 3-Thia-5,8-pentadecadiynoic acid was recrystallized from diisopropyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06511670B1 |
|---|
| Source dataset | uspto-grants-2003_01 |
|---|
| ORD ID | ord-a4e1a1963f764fe3a73082a212fe65c1 |
|---|
| Source note | uspto-grants-2003_01 |
|---|