Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985754Generated: October 30, 2026

Benzaldehyde → HCID 14801250, compound

https://huagongshe.com/reaction/985754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
Reactant1H-PerfluoropropaneHCID 62442—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
ProductHCID 14801250HCID 1480125070%

Reaction Conditions

Temperature-80 °C

Reaction Steps

60 ml of ether and 3.6 g (30 mmol) of 1H-heptafluoropropane were placed in a 4-neck flask fitted with anchor stirrer, dropping funnel, and internal thermometer and the mixture was cooled to −80° C. 9 g (20 mmol) of tert-BuLi as a 15% strength solution in pentane were then added dropwise and the mixture was stirred for another 30 minutes at this temperature. 2.1 g (20 mmol) of benzaldehyde in 10 ml of ether were subsequently added dropwise. After stirring at −80° C. for 2 hours, the yellow solution was allowed to come to room temperature and dilute hydrochloric acid was added. The mixture was extracted three times with ether and the combined organic phases were dried and filtered. Purification by distillation gave heptafluoropropylphenyl alcohol in a yield of 70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872861B2
Source datasetuspto-grants-2005_03
ORD IDord-9c7e8110ac8c4e01a719cf02ac99a3d9
Source noteuspto-grants-2005_03