HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656499Generated: November 1, 2026
2-((Tert-butyldimethylsilyl)oxy)acetaldehyde → HCID 66915419, compound
https://huagongshe.com/reaction/656499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-((Tert-butyldimethylsilyl)oxy)acetaldehyde | HCID 4187788 | — |
| Reactant | HCID 23699784 | HCID 23699784 | — |
| Reactant | HCID 57468508 | HCID 57468508 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66915419 | HCID 66915419 | — |
Reaction Steps
A solution of 1 mol of 3-(3-amino-propyl)-6-methoxy-1,3-dihydro-indol-2-one in 5 ml of ethanol is treated with 5 mmol of sodium acetate hydrochloride and 5 mmol of (tert-butyl-dimethyl-silanyloxy)-acetaldehyde [102191-92-4] and stirred at 60° C. for 3 hours. The reaction mixture is concentrated in vacuo and treated with aqueous saturated potassium carbonate solution and diethyl ether. The phases are separated and the aqueous phase is extracted with diethyl ether (2×). The combined organic phases are washed with water, dried with sodium sulphate and evaporated. From the residue the title compound is identified by means of flash chromatography (SiO2 60F) on the basis of the Rf value.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071774B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-19f03c1c2bf84db39e8cc365266496c7 |
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| Source note | uspto-grants-2011_12 |
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