HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydroxybutanedioate → (2-Heptyloxy-4-iodophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydroxybutanedioate | HCID 3806114 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Methyl 2-heptyloxy-4-iodobenzoate | HCID 68767792 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2-Heptyloxy-4-iodophenyl)methanol | HCID 68768142 | — |
Reaction Steps
A 1M solution of DiBAIH (87.5 ml, 87.5 mmol) is added dropwise to a solution of methyl 2-heptyloxy-4-iodobenzoate obtained in Step a (14 g, 43.7 mmol) in toluene (450 ml), at 0° C. After stirring for 2 hours, a saturated solution of mixed tartrate of sodium and of potassium is added and then the desired product is extracted by addition of ethyl ether. The organic phase is washed with water, dried with magnesium sulfate and concentrated using a rotary evaporator. The product is purified by chromatography on a silica column, eluted with a heptane/ethyl acetate 9:1 mixture. After evaporation of the solvents, 13.64 g (90%) of the expected compound are recovered in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829588B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-9580ae30b3c642ae9037d59be00d6108 |
| Source note | uspto-grants-2010_11 |