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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980323Generated: October 30, 2026

Hydrochloric Acid → HCID 54100633, compound

https://huagongshe.com/reaction/980323

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 soution is obtained. This is cooled to -10° C. and 15-chloro-3-methylene-7,11,15-trimethyl-hexadeca-1,6,10-triene (10 g) are then added followed, over the course of 1 hour, by dry hydrogen chloride gas (3.9 g). The reaction mixture is poured into an aqueous solution (100 cc) of ammonium chloride (100 g/liter). The organic phase is separated off by decanting and the aqueous phase is 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 numberUS04636570
Source datasetuspto-grants-1987_01
ORD IDord-882a0f3bd12148dd831ee947a1943ee5
Source noteuspto-grants-1987_01