HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 6,6,6-trichloro-2,3,3-trimethylhex-4-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 12810690 | HCID 12810690 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 6,6,6-trichloro-2,3,3-trimethylhex-4-enoate | HCID 54466645 | 75% |
Reaction Steps
A solution of 737 mg of ethyl 4-bromo-6,6,6-trichloro-2,3,3-trimethylhexanoate in 20 ml of anhydrous tetrahydrofuran was cooled to 0°. To the cold solution was added 163 mg of sodium ethoxide and the mixture was stirred for 5 hours. The cooled mixture was poured into cold 1N hydrochloric acid and extracted with diethyl ether. The ether extract was washed successively with water, saturated aqueous sodium bicarbonate and aqueous sodium chloride, then dried over magnesium sulfate. The dried ether extract was distilled to give 430 mg (75% yield) of ethyl 6,6,6-trichloro-2,3,3-trimethyl-4-hexenoate, b.p. 92°-95°/0.2 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04999451 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-f6057dd1b7a941458cd57dc50307ee6b |
| Source note | uspto-grants-1991_03 |