Dibenzoylmorphine

Dibenzoylmorphine is an opiate analogue that is a derivative of morphine. It was developed in the early 1900s after first having been synthesised in 1875 in the UK by the CR Alders Wright organisation at Bayer, along with various other esters of morphine, but was never used medically, instead being widely sold as one of the first "designer drugs" for around five years following the introduction of the first international restrictions on the sale of heroin in 1925. It is described as being virtually identical to heroin and morphine in its effects, and consequently was itself banned internationally in 1930 by the Health Committee of the League of Nations, in order to prevent its sale as an unscheduled alternative to diacetylmorphine.[1] However, it still continues to occasionally be encountered as a result of home manufacture from morphine by drug users.[2]

3,6-dibenzoyl-(5α,6α)-7,8-didehydro-4,5-epoxy-17-methylmorphinan

Legal status
Legal status	Illegal under UN drug conventions as "ester of morphine"
Identifiers
IUPAC name [(4R,4Ar,7S,7aR,12bS)-9-benzoyloxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7-yl] benzoate
PubChem CID	58019102
ChemSpider	59650718
Chemical and physical data
Formula	C31H27NO5
Molar mass	493.559 g·mol−1
3D model (JSmol)	Interactive image
SMILES CN1CC[C@]23c4c5ccc(c4O[C@H]2[C@H](C=C[C@H]3[C@H]1C5)OC(=O)c6ccccc6)OC(=O)c7ccccc7
InChI InChI=1S/C31H27NO5/c1-32-17-16-31-22-13-15-25(36-30(34)20-10-6-3-7-11-20)28(31)37-27-24(14-12-21(26(27)31)18-23(22)32)35-29(33)19-8-4-2-5-9-19/h2-15,22-23,25,28H,16-18H2,1H3/t22-,23+,25-,28-,31-/m0/s1 Key:TYRXZVFTBRIZFW-LTQSXOHQSA-N
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It is produced in the same fashion as other esters of morphine—treating morphine with an acid anhydride (or some acids or other relatives of acids like acetyl chloride) to get a mono-, di-, tri-, or tetra-ester. Specifically, the original 1875 synthesis was effected by boiling morphine for 2 hours in benzoic acid at 130 °C, as was heroin made by using acetic anhydride.