HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 53954534, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | HCID 18991514 | HCID 18991514 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53954534 | HCID 53954534 | — |
Reaction Steps
10.5 g (31.3 mmol) of benzyl 6-acetoxy-2-formylamino-3-hydroxy-4-methylenehexanoate are dissolved in 100 ml of abs. CH2Cl2. Then 2.91 ml (37.6 mmol) of thionyl bromide are added to this solution at room temperature. After 2 hours, 80 ml of water are added and the mixture is stirred vigorously for 10 minutes. The organic phase is separated and washed once with water, once with a 1N solution of KHCO3 and twice with water. The aqueous phases are extracted twice with CH2Cl2. The combined organic phases are dried over MgSO4, filtered and concentrated by evaporation, giving benzyl 6-acetoxy-4-bromomethyl-2-formylamino-hex-3-enoate as a yellowish-brown oil which is further reacted without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05488140 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-d1abd21329a3421c8a4f5dffc82315e9 |
| Source note | uspto-grants-1996_01 |