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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376177Generated: October 30, 2026

Dichloromethane → HCID 53954534, compound

https://huagongshe.com/reaction/376177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantThionyl bromideHCID 68176—
ReactantHCID 18991514HCID 18991514—
SolventWaterHCID 962—
ProductHCID 53954534HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488140
Source datasetuspto-grants-1996_01
ORD IDord-d1abd21329a3421c8a4f5dffc82315e9
Source noteuspto-grants-1996_01