HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582902Generated: October 30, 2026
Sodium borohydride → HCID 10902156, compound
https://huagongshe.com/reaction/582902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 56999066 | HCID 56999066 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10902156 | HCID 10902156 | 75% |
Reaction Steps
In 500 ml of tetrahydrofuran were suspended 62.4 g (0.2 mol) of the methyl (2S,3R)-2,3-epoxyoctadecanoate (V-1) prepared in Example 3-(3) and 7.4 g (0.2 mol) of NaBH4, followed by heat refluxing for 3 hours. After confirming disappearance of the compound (V-1) by TLC, tetrahydrofuran was evaporated. To the residue were added 20 ml of water and then 500 ml of a saturated ammonium chloride aqueous solution to adjust to pH 5 to 6, and the mixture was extracted with 500 ml of ethyl acetate. After drying, ethyl acetate was removed by evaporation, and the resulting crude crystals were recrystallized from heptane to obtain 42.6 g (0.15 mol; yield: 75%) of (2R,3R)-2,3-epoxyoctadecanol (melting point: 77 to 78° C.). Optical rotation [α]D25 =+24.5° (c=0.285, CHCl3)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05925792 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-0b1b40ca4bb641a3a0d2421a717da038 |
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| Source note | uspto-grants-1999_07 |
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