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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246Generated: October 26, 2026

Trimethyl orthoacetate → Methyl 6-bromo-6-chloro-3,3-dimethyl-7,7,7-trifluorohept-4-enoate

https://huagongshe.com/reaction/1246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoacetateHCID 15050—
Reactant1,1,1-Trifluoro-2-bromo-2-chloro-5-methyl-4-hexen-3-olHCID 15219346—
CatalystBentoniteHCID 71586775—
ProductMethyl 6-bromo-6-chloro-3,3-dimethyl-7,7,7-trifluorohept-4-enoateHCID 5445106765%

Reaction Conditions

Temperature111 °C

Reaction Steps

5-Bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene (10.0 g), trimethyl orthoacetate (16.0 g) and Montmorillonite KSF (0.5 g) were charged to a round-bottomed flask fitted with: nitrogen inlet/bubbler, thermometer and still-head. The mixture was heated with agitation, and the methanol-trimethyl orthoacetate distillates were collected until the reactor temperature increased to 111° C. (ca. 1 hr). The reaction was then heated to 135° C. and held for a further 1 hour. The methanol/trimethyl orthoacetate distillates were recharged and the distillation procedure repeated twice. Once the reaction was complete, the Montmorillonite was removed by filtration. The residual trimethyl orthoacetate was then removed by distillation under vacuum (ca. 50° C. @ 100 mmHg) to give the product, methyl 6-bromo-6-chloro-3,3-dimethyl-7,7,7-trifluorohept-4-enoate as a brown oil (7.8 g, 59% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723649
Source datasetuspto-grants-1998_03
ORD IDord-d60f1ea20aa0467e8d0f2bb79c4451e3
Source noteuspto-grants-1998_03