HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium tri-s-butylborohydride → 5-Bromo-1-methoxy-3-methyl-8-(1-methylethoxy)naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| Reactant | HCID 15341856 | HCID 15341856 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-1-methoxy-3-methyl-8-(1-methylethoxy)naphthalene | HCID 11055969 | 98% |
Reaction Steps
To a 0° C. cold solution of 7.60 g (19.6 mmol) 1-bromo-7-bromomethyl-4-isopropoxy-5-methoxy-naphthalene in 150 mL dry dichloromethane, 20.0 mL (20.0 mmol) of a 1M L-selectride-solution was added under Ar. After 2 h, further 2.50 mL (2.50 mmol) 1M L-selectride-solution was added. After that the solvent was removed in vacuo and the residue was filtered over a short silica gel column (petroleum/acetone, 30:1). After removal of the solvent in vacuo, the residue was recrystallized from acetone to give 5.90 g (98%) of 4 as colorless needles (m.p. 78° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05552550 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-329465121cd744e299358f5deaf45108 |
| Source note | uspto-grants-1996_09 |