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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982433Generated: October 30, 2026

1-Bromo-3-chloropropane → HCID 12338059, compound

https://huagongshe.com/reaction/982433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
Reactant2-PhenylacetophenoneHCID 9948—
ProductHCID 12338059HCID 12338059—

Reaction Steps

In the first stage 19.6 g of desoxybenzoin is alkylated with 15.8 g of 3-bromo-1-chloropropane according to the procedure described in method 1 except that the reaction is carried out at room temperature. Isolation gives an intermediate, 2,3-diphenyl-4,5-dihydro-6H-pyran in quantitative yield, but the product contains about 10% of noncyclic O-alkylation product. The m.p. of a sample which has been chromatographically purified and recrystallized from methanol is 119°-22° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04996225
Source datasetuspto-grants-1991_02
ORD IDord-d323962ce7534018b4488e6ef2bf4aa6
Source noteuspto-grants-1991_02