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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978911Generated: October 29, 2026

Hydrochloric Acid → HCID 54100633, compound

https://huagongshe.com/reaction/978911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 54312390HCID 54312390—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 54100633HCID 5410063396.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Triethylamine hydrochloride (0.48 g), methylene chloride (15 cc), acetic acid (10 cc) and cuprous chloride (90 mg) are introduced, under an argon atmosphere, into a 250 cc reactor. The reaction mixture is stirred until a homogeneous solution is obtained. This is cooled to -10° C. and 15-chloro-3-methylene-7,11,15-trimethyl-hexadeca-1,6,10-triene (10 g) is then added followed, over the course of 1 hour, by dry gaseous hydrogen chloride (3.9 g). The reaction mixture is poured into an aqueous solution (100 cc) of ammonium chloride (100 g/liter). The organic phase is removed by decanting and the aqueous phase is then extracted with methylene chloride (twice 100 cc). The combined organic phases are washed with water (100 cc) and then dried over potassium carbonate. After filtration and evaporation of the solvent, 1,7,11,15-tetrachloro-3,7,11,15-tetramethyl-hexadec-2-ene (13.1 g) is obtained in a yield of 96.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665244
Source datasetuspto-grants-1987_05
ORD IDord-46518c3778784b6bb7170c4be0757af1
Source noteuspto-grants-1987_05