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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939367Generated: October 30, 2026

1-(Bromomethyl)-3-chlorobenzene → HCID 53708608, compound

https://huagongshe.com/reaction/1939367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantPotassium BromideHCID 253877—
ReactantHCID 54418906HCID 54418906—
SolventHexaneHCID 8058—
ProductHCID 53708608HCID 53708608—

Reaction Steps

Prepared from 2-(2-tert-butyldimethylsiloxyethyl)-6-carbomethoxy-3,4-dihydro-3-oxo-2H-1,4-benzoxazine by Methods F and G, alkylating with 3-chlorobenzyl bromide, in 70% overall yield as a white solid, after trituration with hexane, IR (KBr) 3468, 2952, 1688, 1452, 1285, 1260, 765 cm-1 ; 1H NMR (CDCl3) δ1.61 (br s, 1H plus HDO), 2.17-2.39 (m, 2H), 3.86 (s, 3H), 3.93 (t, J=5.7 Hz, 2H), 4.94 (dd, J=7.6, 5.5 Hz, 1H), 5.16 (s, 2H), 7.04 (d, J=8.4, 1H), 7.15-7.33 (m, 4H), 7.59 (d, J=1.8 Hz, 1H), 7.71 (dd, J=8.4, 1.8 Hz, 1H); MH+ at m/z=376; Anal. Calc'd for C19 H18ClNO5.0.1H2O: C, 60.44; H, 4.86; N, 3.71. Found: C, 60.26; H, 4.60; N, 3.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696117
Source datasetuspto-grants-1997_12
ORD IDord-0c67b8f6698d4e4bb8390e00c92d722d
Source noteuspto-grants-1997_12