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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,1-Dimethyl-2-hydroxy-2-(3,4-methylenedioxyphenyl)nitroethane | HCID 23454852 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-(1-Chloro-2-methyl-2-nitropropyl)-2H-1,3-benzodioxole | HCID 23454839 | 79.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04073798 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-23e2ec6f8c4c4aa385ddd71e7fd8a971 |
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| Source note | uspto-grants-1978_02 |
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