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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742102Generated: October 31, 2026

Lithium tri-s-butylborohydride → 5-Bromo-1-methoxy-3-methyl-8-(1-methylethoxy)naphthalene

https://huagongshe.com/reaction/742102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium tri-s-butylborohydrideHCID 3611392—
ReactantHCID 15341856HCID 15341856—
SolventDichloromethaneHCID 6344—
Product5-Bromo-1-methoxy-3-methyl-8-(1-methylethoxy)naphthaleneHCID 1105596998%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552550
Source datasetuspto-grants-1996_09
ORD IDord-329465121cd744e299358f5deaf45108
Source noteuspto-grants-1996_09