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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067334Generated: October 31, 2026

Thionyl Chloride → tert-Butyl [4-(chloromethyl)phenyl]carbamate

https://huagongshe.com/reaction/2067334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantBoc-4-aminobenzylalcoholHCID 10242688—
CatalystPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Producttert-Butyl [4-(chloromethyl)phenyl]carbamateHCID 4683524950%

Reaction Steps

To a stirred solution of tert-butyl 4-(hydroxymethyl)phenylcarbamate (0.50 g, 2.24 mmol) in dichloromethane was added pyridine (3 drops), followed by the dropwise addition of thionyl chloride (0.35 mL, 4.98 mmol). The resulting reaction mixture was stirred for 30 minutes, and then quenched with water (25 mL). The aqueous layer was extracted with dichloromethane (50 mL), and the organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to afford tert-butyl 4-(chloromethyl)-phenylcarbamate as an orange solid in 50% yield (0.27 g, 50%): 1H NMR (300 MHz, CDCl3) δ 7.38-7.28 (m, 4H), 6.51 (br s, 1H), 4.55 (s, 2H), 1.52 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293768B2
Source datasetuspto-grants-2012_10
ORD IDord-3e98fc89cd874f068a4dfc2132c2176b
Source noteuspto-grants-2012_10