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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115991Generated: October 31, 2026

Benzyl chloroformate → HCID 86599220, compound

https://huagongshe.com/reaction/2115991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11960945HCID 11960945—
ProductHCID 86599220HCID 8659922081%

Reaction Steps

Treatment of (±)-(5-chloro-7-thien-3-yl-2,3-dihydro-1-benzofuran-2-yl)methylamine (2.45 g, 8.11 mmol) with benzyl chloroformate (2.07 g, 12.15 mmol) and diisopropylethylamine (3.43 g, 24.32 mmol) generally according to the procedure described for Intermediate 12 provided 2.6 g (81%) of (±)-benzyl(5-chloro-7-thien-3-yl-2,3-dihydro-1-benzofuran-2-yl)methylcarbamate as a white solid. mp 90-92° C.; Anal. calcd. for C21H18ClNO3S: C, 63.07; H, 4.54; N, 3.50. Found: C, 63.44; H, 4.51; N, 3.43. Chiral HPLC separation of (±)-benzyl(5-chloro-7-thien-3-yl-2,3-dihydro-1-benzofuran-2-yl)methylcarbamate (Chiralpak AD, hexane:ethanol 1:1) provided two fractions. Fraction 1 (Rt=11.538 min, (Chiralpak AD, hexane:ethanol 1:1); Fraction 2 (Rt=17.694 min, (Chiralpak AD, hexane:ethanol 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-37826cedbde94d1f82d28a64d503b7e9
Source noteuspto-grants-2008_10