Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 85701945 | HCID 85701945 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54541172 | HCID 54541172 | — |
Reaction Steps
5 g (16.4 mmol) monocitronellyl (+)-phthalate was heated at reflux in 25 ml oxalyl chloride (18 eq.) for 3 h. The excess oxalyl chloride was distilled under vacuum. 5.3 g crude acid chloride was then diluted in 40 ml THF cooled to −8° under argon, and 1.87 g (3 eq.) NaBH4 was added. The reaction mixture was maintained under stirring at 0° for 4 h, then at ambient temperature for 16 h. The reaction mixture was then cooled again to 0°, and then 10 ml methanol was added dropwise. After 15 min, the mixture was poured over cold 5% KHSO4 then extracted using cold ethyl acetate. Chromatography of the crude product over silica gel (9:1 toluene/ether) yielded 1.41 g (31%) of almost pure 3,7-dimethyl-6-octenyl 2-hydroxymethylbenzoate in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06589921B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-5d3986bc4b6a401181d831027fa6d1ef |
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| Source note | uspto-grants-2003_07 |
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