HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 21312640, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21312609 | HCID 21312609 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21312640 | HCID 21312640 | — |
Reaction Steps
A solution of 5.5 g of sodium borohydride in 50 ml. of 95% ethanol is added to a solution of the compound of formula VI, dimethyl trans-2-(3-oxo-1-octenyl)cyclopropane-1,1-dicarboxylate (35 g), described in Example 2. After 15 min. at room temperature the mixture is cooled in ice and rendered neutral by the addition of acetic acid. Water is added and the mixture extracted with ethyl-acetate. The extract was dried (Na2SO4) and the evaporated. The residue is purified by chromatography on silica gel to afford the title compound, nmr (CDCl3) δ 0.90 (t, 3H), 2.33 (1H), 3.73 (s, 3H) 4.05 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04161608 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-ee9e4eb765d54328a3648b858bc01a95 |
| Source note | uspto-grants-1979_07 |