HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644568Generated: October 30, 2026
3-(t-Butyldimethylsilyloxy)benzaldehyde → 1-[3-(tert-Butyldimethylsilanyloxy)phenyl]propan-1-ol
https://huagongshe.com/reaction/644568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(t-Butyldimethylsilyloxy)benzaldehyde | HCID 11207111 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[3-(tert-Butyldimethylsilanyloxy)phenyl]propan-1-ol | HCID 68579551 | — |
Reaction Steps
50 g (0.21 mol) of 3-(tert-butyldimethyl-silanyloxy)benzaldehyde are dissolved in 500 ml of ethyl ether and the mixture is cooled to 0° C. 80 ml (0.24 mol) of a 3.0 M solution of ethylmagnesium bromide are added slowly, and the mixture is stirred for 5 hours. After the usual treatment, the residue obtained is purified by chromatography on a silica column (eluent ethyl acetate 20/hexane 80). A colorless oil is obtained (m=45.8 g; Y=82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700657B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-4b4a01cb649a4491bf392461ba2c5fac |
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| Source note | uspto-grants-2010_04 |
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