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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115958Generated: November 4, 2026

Benzyl chloroformate → HCID 86599137, compound

https://huagongshe.com/reaction/2115958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11960767HCID 11960767—
ProductHCID 86599137HCID 8659913787.2%

Reaction Steps

Treatment of (±)-1-[7-(2,6-dimethylphenyl)-2,3-dihydro-1-benzofuran-2-yl]methanamine (0.947 g, 3.73 mmol) with diisopropylethylamine (0.725 g, 5.60 mmol) and benzyl chloroformate (0.7647 g, 4.48 mmol) generally according to the procedure described for Intermediate 12 gave 1.26 g (87%) of (±)-benzyl[7-(2,6-dimethylphenyl)-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate as a colorless oil Rf=0.56 (silica, ethyl acetate:hexanes 1:4); Anal. calcd. for C25H25NO3: C, 77.49; H, 6.50; N, 3.61. Found: C, 77.42H, 6.57; N, 3.62. Chiral HPLC separation of (±)-benzyl[7-(2,6-dimethylphenyl)-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate (Chiralcel OJ, methanol:carbon dioxide 4:6) provided two fractions. Fraction 1 (Rt=2.89 min, Chiralcel OJ, methanol:carbon dioxide 4:6); Fraction 2 (Rt=3.84 min, Chiralcel OJ, methanol:carbon dioxide 4:6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-566e757354b54c10b296bef63f93dc44
Source noteuspto-grants-2008_10