HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450776Generated: October 30, 2026
4-Hydroxybenzyl Alcohol → HCID 59478957, compound
https://huagongshe.com/reaction/450776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59478957 | HCID 59478957 | — |
Reaction Steps
To a mixture of 2.97 g of 4-(hydroxymethyl)phenol, 4.90 g of tert-butyl bromoacetate, and 25 ml of DMF was added 4.96 g of potassium carbonate at room temperature, followed by stirring for 12 hours. To the reaction solution was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was then evaporated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate-hexane) to obtain a pale yellow oily substance. This oily substance was subjected to methanesulfonylation in accordance with Production Example 15, and then reacted with sodium azide to obtain 4.03 g of tert-butyl[4-(azidomethyl)phenoxy]acetate as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486970B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-2d3e493ec6c04292bbb67fc574b44c89 |
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| Source note | uspto-grants-2013_07 |
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