HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butyne-1,4-diol → Methyl [(4-hydroxybut-2-yn-1-yl)oxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butyne-1,4-diol | HCID 8066 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3-bromopropanoate | HCID 76934 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl [(4-hydroxybut-2-yn-1-yl)oxy]acetate | HCID 53999001 | 35% |
Reaction Steps
Sodium hydride (60% dispersion in oil, 2.32 g, 58 mmol) was added to a solution of 2-butyne-1,4-diol (5.0 g, 58 mmol) in THF (60 mL) at 0° C. under nitrogen. After 1 h at 0° C., methyl bromomethylacetate (5.5 mL, 58 mmol) was added and the reaction was allowed to warm to rt. After 18 h at rt, the reaction was quenched with 1 N HCl (60 mL) and extracted with EtOAc (3×100 mL). The combined extracts were washed with brine (1×100 mL), dried (MgSO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→5% MeOH/CH2Cl2, gradient) afforded 3.2 g (35%) of (4-hydroxy-but-2-ynyloxy)-acetic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179820B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-ef0148b150e840c5a4174154adc19643 |
| Source note | uspto-grants-2007_02 |