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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807341Generated: October 30, 2026

Hydrochloric Acid → HCID 66974036, compound

https://huagongshe.com/reaction/1807341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAllyl AlcoholHCID 7858—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHCID 66974043HCID 66974043—
CatalystMethanesulfonic AcidHCID 6395—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 66974036HCID 6697403625.4%

Reaction Steps

Hydrochloric acid (HCl, 6 g) was added to a solution of 1,4-dimethyl-bicyclo[3.2.1]octan-3-one (400 g, 2.6 mol, obtained as above in EXAMPLE III), trimethylorthoformate (HC(OCH3)3, 280 g, 2.6 mol), and methanol (CH3OH, 400 mL). The reaction mixture was aged for 3 hours and subsequently quenched with a NaOH solution. Allyl alcohol (CH2CHCH2OH, 300 g, 5.2 mol), acetic acid (CH3COOH, 50 g), and methanesulfonic acid (CH3SO2OH, MSA, 5 g) were added and aged at reflux. The volatile ingredients were distilled off with a Dean Stark trap. The resulting mixture was washed with a Na2CO3 solution. Fractional distillation of the organic layer provided 4-allyl-1,4-dimethyl-bicyclo[3.2.1]octan-3-one (127 g) having a boiling point of 64° C. at a pressure of 0.2 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357358B2
Source datasetuspto-grants-2013_01
ORD IDord-313c33beba9e459a9fa8af328918919c
Source noteuspto-grants-2013_01