HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzyl alcohol → HCID 22645476, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzyl alcohol | HCID 102 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22645476 | HCID 22645476 | — |
Reaction Steps
To a solution of 3-(hydroxymethyl)-phenol (50 g, 0.4 mol) and t-butyl bromoacetate (86 g, 0.44 mol) in DMF (500 ml, anhydrous) at room temperature is added K2CO3 (122 g, 0.88 mol). The reaction mixture is stirred vigorously for 2 hrs, and the mixture is poured into ice-water (2.5 L) and extracted with ether (3×500 ml). The combined ether extracts are washed with water, dried over MgSO4 and evaporated in vacuo to provide t-butyl-3-(hydroxymethyl)-phenoxyacetate as a low melting, light yellow solid; mp: 52-56° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06812237B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-3295823a5684449cad72d580ca694b4c |
| Source note | uspto-grants-2004_11 |