HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728411Generated: October 31, 2026
Benzaldehyde → (1S)-1-Phenylbut-3-en-1-ol
https://huagongshe.com/reaction/728411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Catalyst | Titanium | HCID 23963 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1S)-1-Phenylbut-3-en-1-ol | HCID 6993460 | 66% |
Reaction Steps
A solution of 1.25 mmol of the titanium compound of Example 2b in 60 ml of diethyl ether is cooled to -74° C., and 0.1 ml (1.0 mmol) of freshly distilled benzaldehyde is added. The slightly yellow, clear solution is stirred for a further 2 hours at -74° C. and 5 ml of a 5N H2O/THF solution are added and the mixture is warmed to RT, stirred for a further hour at this temperature, filtered with suction and concentrated on a rotary evaporator. The crude product (0.80 g of a clear colourless oil) is flash-chromatographed (60 g of silica gel, 35 cm long, cross-section 2 cm, 5 ml/fraction, 0.4 bar, 10:1 toluene/ethanol). 0.098 g of product is obtained. Yield: 66%, ee: 93%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047557 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-7c4fbac6ba2a46c3b2da02bcc8711943 |
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| Source note | uspto-grants-1991_09 |
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