HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2R)-3-Benzyloxymethoxy-2-methyl-propionic acid methyl ester → (2R)-3-Benzyloxymethoxy-2-methyl-propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2R)-3-Benzyloxymethoxy-2-methyl-propionic acid methyl ester | HCID 10082905 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R)-3-Benzyloxymethoxy-2-methyl-propan-1-ol | HCID 11805955 | 66% |
Reaction Steps
A solution of ester 2 (0.5 g, 2.1 mmol) in anhydrous THF (4 mL) was added dropwise to a suspension of lithium aluminum hydride (0.16 g, 4.2 mmol) in anhydrous THF (10 mL) at 0° C. The cooling bath was removed, and the reaction was stirred at room temperature overnight, quenched with cold water, and extracted with EtOAc. The solvents were removed in vacuum and the crude oil was purified by silica gel chromatography using hexane/EtOAc (8:2) as an eluent to afford oily diol 3 (0.29 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534777B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-1f9a45735dff4d48a12b89eb30b2f784 |
| Source note | uspto-grants-2009_05 |