Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585598Generated: October 26, 2026

Sodium hydride → 2-amino-5-(Benzothiazol-2-ylmethoxy)-naphthalene

https://huagongshe.com/reaction/585598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant6-AminonaphtholHCID 90295—
Reactant2-(Bromomethyl)-1,3-benzothiazoleHCID 2776258—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-amino-5-(Benzothiazol-2-ylmethoxy)-naphthaleneHCID 2233784415%

Reaction Steps

Sodium hydride (1.05 g) is added to a cooled solution of 2-Amino-5-naphthol (4.18 g) in dimethylformamide (100 mL). Stir at room temperature 15 minutes and cool mixture. 2-Bromomethylbenzothiazole (6.00 g) is added and mixture to allowed to warm slowly and stir for 24 hours. Remove dimethylformamide in vacuo. Redilute with ethylacetate and absorb onto silica gel. Chromatograph (ethyl acetate/hexane) to give a brown solid (1.20 g, 15%) which was used directly in the next step., m.p. 141-143° C. 1H NMR (DMSO-d6, 400 MHz): d 5.43 (br s, 2H), 5.69 (s, 2H), 6.72 (d, 1H), 6.80 (s, 1H), 6.95 (d, 1H), 7.12-7.20 (m, 2H), 7.45 (t, 1H), 7.54 (t, 1H), 7.97 (d, 1H), 8.02 (d, 1H), 8.14 (d, 1H). MS [EI, m/z]: 306 [M]+. Anal. Calcd. for C18H14N2OS: C, 70.56; H, 4.61; N, 9.14. Found: C, 70.38; H, 4.42; N, 9.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933322B2
Source datasetuspto-grants-2005_08
ORD IDord-c1f8f064938c45a98ca03e770979bd78
Source noteuspto-grants-2005_08