関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Ethylenediamine | HCID 3301 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 3-Dodecynoic acid, 11-hydroxy- | HCID 10899930 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Nickel Acetate | HCID 9756 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Sodium Hydroxide | HCID 14798 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | 11-hydroxy-3Z-dodecenoic acid | HCID 86740560 | 96.4% |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04560551 |
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| 出典データセット | uspto-grants-1985_12 |
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| ORD ID | ord-6d96527de97c44c283ca96f9c8228bd4 |
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| 出典メモ | uspto-grants-1985_12 |
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