HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → {4-[2-(Benzyloxy)ethoxy]-3-tert-butoxyphenyl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-[2-(Benzyloxy)ethoxy]-3-tert-butoxybenzaldehyde | HCID 89156229 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {4-[2-(Benzyloxy)ethoxy]-3-tert-butoxyphenyl}methanol | HCID 70978543 | — |
Reaction Steps
To a stirred mixture of 1.00 g (26.5 mmol) sodium borohydride in 80 ml THF was added 2, 0.9 g (8.83 mmol) 4-[2-(benzyloxy)ethoxy]-3-tert-butoxybenzaldehyde diluted in 40 ml THF drop by drop. The reaction mixture was stirred for 10 min. Methanol (5.8 ml) was added to this mixture drop by drop. The reaction mixture was stirred for 2 hours and poured onto ˜200 ml stirred ice-cooled saturated aqueous ammonium chloride solution. The solution was extracted trice with dichloromethane. The combined organic phases were dried with sodium sulfate and concentrated in vacuo. The crude product was used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238631B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-11d45f88025b4d879dc660c4ca8f9a5a |
| Source note | uspto-grants-2016_01 |