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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638140Generated: October 25, 2026

Hydrochloric Acid → 11-hydroxy-3Z-dodecenoic acid

https://huagongshe.com/reaction/638140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylenediamineHCID 3301—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Dodecynoic acid, 11-hydroxy-HCID 10899930—
ReactantHCID 178418361HCID 178418361—
CatalystNickel AcetateHCID 9756—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
SolventSodium chloride; waterHCID 57417360—
Product11-hydroxy-3Z-dodecenoic acidHCID 8674056096.4%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a vigorously stirred mixture of nickel acetate (1 g) and absolute ethanol (25 mL), saturated with hydrogen, was added 5 mL of the filtrate from a solution of sodium borohydride (500 mg) in ethanol (12 mL) and 2N aqueous sodium hydroxide (0.63 mL). After hydrogen evolution had ceased, the black suspension was treated with 0.7 mL of ethylene diamine.6Alkyne 24 (643 mg, 3.0 mmol) was added and the reaction stirred for 1 hr at 23° C. The reaction was diluted with brine (100 mL), acidified with 5% HCl and extracted with ether (4×50 mL). The ether extract was washed with brine (2×50 mL). Product isolation gave 620 mg of 26 (96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560551
Source datasetuspto-grants-1985_12
ORD IDord-6d96527de97c44c283ca96f9c8228bd4
Source noteuspto-grants-1985_12