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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115946Generated: October 31, 2026

Benzyl chloroformate → HCID 91432033, compound

https://huagongshe.com/reaction/2115946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 69274359HCID 69274359—
ProductHCID 91432033HCID 91432033—

Reaction Steps

Treatment of (±)-benzyl(7-phenyl-2,3-dihydro-1-benzofuran-2-yl)methanamine (1.5 g, 1.43 mmol) with diisopropylethylamine (0.277 g, 2.14 mmol) followed by benzyl chloroformate (0.268 g, 1.572 mmol) generally according to the procedure described for Intermediate 12 provided 1.64 (79%) of (±)-benzyl[7-phenyl-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate as a clear oil. Rf=0.68 (silica, ethyl acetate:hexanes 1:2); Anal. calcd. for C23H21NO3: C, 76.86; H, 5.89; N, 3.90. Found: C, 75.10H, 5.71; N, 3.90. Chiral HPLC separation of (±)-benzyl[7-phenyl-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate (Chiralpak AD, ethanol:hexane 1:1) provided two fractions. Fraction 1 (Rt=10.746 min, Chiralpak AD, ethanol:hexane 1:1); Fraction 2 (Rt=13.433 min, Chiralpak AD ethanol:hexane 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-de5ea3faf1dc4f329eedc7e98e9b8092
Source noteuspto-grants-2008_10