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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Dodecynoic acid, 11-hydroxy- | HCID 10899930 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel Acetate | HCID 9756 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 11-hydroxy-3Z-dodecenoic acid | HCID 86740560 | 96.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560551 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-6d96527de97c44c283ca96f9c8228bd4 |
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| Source note | uspto-grants-1985_12 |
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