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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616257Generated: October 30, 2026

Methane → 5-(1-Chloro-2-methyl-2-nitropropyl)-2H-1,3-benzodioxole

https://huagongshe.com/reaction/616257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantThionyl ChlorideHCID 24386—
Reactant1,1-Dimethyl-2-hydroxy-2-(3,4-methylenedioxyphenyl)nitroethaneHCID 23454852—
SolventBenzeneHCID 241—
Product5-(1-Chloro-2-methyl-2-nitropropyl)-2H-1,3-benzodioxoleHCID 2345483979.6%

Reaction Steps

A solution of 242.8 g (1.016 moles) of 1,1-dimethyl-2-hydroxy-2-(3,4-methylenedioxyphenyl)nitroethane in 500 ml of benzene was treated with 139 g (84 ml, 1.17 moles) of thionyl chloride, after which the mixture was refluxed for 4 hours, cooled slightly and concentrated to a dark yellow oil which crystallised on cooling and seeding. The resulting solid was broken up and dispersed in 150 ml of 2-propanol after which it was separated, washed twice with cold 2-propanol and dried to give crude 1,1-dimethyl-2-chloro-2-(3,4-methylenedioxyphenyl)nitroethane as a light yellow solid, m.p. 63°-66° C (Yield 230.9 g). A 201.3 g portion of the crude product was treated with "Darco" (Trade Mark) and recrystallised from 402 ml of SDA-30 to give 181.6 g (79.6%) of the pure product as a white solid, m.p. 65°-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04073798
Source datasetuspto-grants-1978_02
ORD IDord-23e2ec6f8c4c4aa385ddd71e7fd8a971
Source noteuspto-grants-1978_02