Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 250219Erstellt: 27. Oktober 2026

Hydrochloric Acid → 5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxole

https://huagongshe.com/reaction/250219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktFormaldehydeHCID 712—
EduktDichloromethaneHCID 6344—
Edukt1,3-Benzodioxole, 5-methyl-HCID 81564—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelDiethyl EtherHCID 3283—
Produkt5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxoleHCID 1055941662%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

At about 0° C., 5-methylbenzo[d][1,3]dioxole (500 mg, 3.68 mmol) and formaldehyde (37% in water, 0.7 mL) were sequentially added to a mixture of dichloromethane (6.8 mL), tetrabutylammonium bromide (80 mg) and concentrated hydrochloric acid (6.5 mL). Under continuous stirring, the mixture was maintained at about 0° C. for about 1 hour and then at ambient temperature for about 4 hours. The mixture was diluted with ether (100 mL). After standard extractive workup, the resulting solid residue was heated with hexanes (100 mL) and the insolubles were removed by filtration. The filtrate was concentrated to give desired product (420 mg, 62%). 1H NMR (300 MHz, CDCl3) δ 6.89 (s, 1H), 6.69 (s, 1H), 5.94 (s, 3H), 4.56 (s, 2H), 2.35 (s, 3H); GC-MS: m/z=184 (MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863308B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-b6b6d050f2924effa5aa7dbff1654bc5
Quellennotizuspto-grants-2011_01