HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242789Generated: November 2, 2026
Chloromethyl Methyl Ether → HCID 68741732, compound
https://huagongshe.com/reaction/2242789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | HCID 13164942 | HCID 13164942 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68741732 | HCID 68741732 | 57% |
Reaction Steps
A solution of diisopropylamine (13.1 mL) in THF was treated dropwise with butyl lithium (58.4 mL of 1.6M solution in hexanes) at −10° C. Then the reaction mixture was cooled to −70° C. and treated dropwise with 2-isopropyl-γ-butyrolactone (9.30 mL) keeping the speed of the addition at such a rate that the temperature of the mixture remained below −60° C. After completion of the addition, the mixture was stirred for 3 h at −70° C., then warmed-up to −40° C. and treated dropwise at this temperature with chloromethyl methyl ether (7.50 mL). After that, the mixture was allowed to slowly warm-up to room temperature and stirred at this temperature for 80 h. The solvents were removed in vacuum and the residue was redissolved in dichloromethane, then washed with a saturated aqueous solution of ammonium chloride, dried over magnesium sulfate, filtered, concentrated on a rotary evaporator and distilled in vacuum to give 7.00 g (57%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07674741B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-8d3a08b3f2f34d248a897b1303283644 |
|---|
| Source note | uspto-grants-2010_03 |
|---|