Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439833Generated: October 30, 2026

Benzothiazole → HCID 22408313, compound

https://huagongshe.com/reaction/439833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
Reactant3-MethylbutanalHCID 11552—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22408313HCID 2240831318%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of n-butyllithium (2.5M in hexanes; 65.1 ml, 0.163 mol) was added to a stirred solution of benzothiazole (20.0 g, 0.148 mol) in dry THF (250 ml) under argon at -78° C. After 10 min a solution of isovaleraldehyde (17.4 ml, 0.163 mol) in dry THF (50 ml) was added slowly and the mixture stirred for 1 h at -78° C. The reaction mixture was removed from the cooling bath and after 10 min was quenched by the addition of excess water and the mixture extracted with ethyl acetate. The combined organic layers were washed with water, dried, filtered and evaporated. Chromatography (20-30% diethyl ether in hexane) gave 1-(2-benzothiazolyl)-3-methylbutanol (5.8 g, 18%) as an amorphous yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516783
Source datasetuspto-grants-1996_05
ORD IDord-eb766bb3b7b94866b7531316bf807908
Source noteuspto-grants-1996_05