HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376972Generated: October 28, 2026
3-Chloro-2-methyl-1-propene → HCID 11726907, compound
https://huagongshe.com/reaction/1376972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,6-DI-Tert-butyl-4-hydroxyphenyl acetate | HCID 11139998 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11726907 | HCID 11726907 | 90% |
Reaction Steps
60% Oily sodium hydride (0.18 g) was suspended in N,N-dimethylformamide (16 ml). A solution of 4-acetoxy-3,5-di-tert-butylphenol (1 g) in N,N-dimethylformamide (5 ml) was added dropwise to the suspension under ice cooling and the mixture was stirred for 30 min. Subsequently, the reaction mixture was allowed to warm to room temperature and 3-chloro-2-methyl-1-propene (0.45 ml) was added dropwise. After stirring at room temperature for 2 h, a saturated aqueous solution of ammonium chloride (15 ml) was added to the reaction mixture. The mixture was subjected to extraction with diethyl ether and the organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 4-acetoxy-3,5-di-tert-butyl-1-(2-methyl-2-propenyloxy)benzene [1.08 g (yield, 90%)] as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05663373 |
|---|
| Source dataset | uspto-grants-1997_09 |
|---|
| ORD ID | ord-0a4f223d74a44214baf3ca06a2c6caab |
|---|
| Source note | uspto-grants-1997_09 |
|---|